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Pitocin

oxytocin · Injection

Prescription NDA TE AP RLD Official labelling
Informational index, not medical advice. Content is reproduced from public FDA and NLM data. Always confirm against the manufacturer's current prescribing information. Report adverse events to FDA MedWatch.

Overview

Brand name
Pitocin
Generic name
oxytocin
Dosage form
Injection
Route
Intravenous
Marketing category
NDA · NDA
Labeler
Par Health USA, LLC
Product type
Human Prescription Drug
DEA schedule
Not scheduled
Active ingredients
1
NDC product codes
2
Packages
6
Data completeness
77% of corroborating sources present

Active ingredients

Source: NDC Directory
Active ingredients and strengths as listed in the NDC Directory.
Ingredient Strength RxCUI Monograph
Oxytocin 10 [iU]/mL 207315 View

Forms, strengths and routes

Source: NDC Directory
Dosage form
Injection
Route of administration
Intravenous
Presentations
8

Pharmacologic classes are listed in the class section below.

Pharmacologic class

Source: NDC Directory
Established pharmacologic classes (EPC), mechanisms of action (MoA), chemical structures (CS) and physiologic effects (PE).
Class Type Browse
Increased Uterine Smooth Muscle Contraction or Tone [PE] PE 3 members — no class page
Oxytocic [EPC] EPC 3 members — no class page
Oxytocin [CS] CS 3 members — no class page

Regulatory status

Source: Drugs@FDANDC Directory
Application number
018261
Application type
NDA · New Drug Application
Approval date
November 19, 1980
Sponsor
PH HEALTH
Products on application
3
Submissions recorded
28
Products approved under application 018261.
Product Trade name Form Strength Ingredient Status TE Flags
018261-001 PITOCIN INJECTABLE OXYTOCIN Prescription AP RLD RS
018261-002 PITOCIN INJECTABLE OXYTOCIN Prescription AP RLD
018261-003 PITOCIN INJECTABLE OXYTOCIN Prescription — RLD

Therapeutic equivalence

Source: Orange Book
TE code
AP
Reference Listed Drug
Yes
Reference Standard
Yes

What this rating means: Therapeutically equivalent — bioequivalence demonstrated (parenteral aqueous solutions)

Codes beginning with “A” indicate products the FDA considers therapeutically equivalent. Codes beginning with “B” indicate bioequivalence has not been established. See methodology.

Approval history

Source: Drugs@FDA
Most recent submissions on application 018261.
Type No. Action Status Date Review
Supplement 41 Labeling Approved May 11, 2021 Standard
Supplement 33 Manufacturing (CMC) Approved August 15, 2016 N/A
Supplement 31 Labeling Approved October 2, 2014 Standard
Supplement 32 Manufacturing (CMC) Approved June 18, 2014 Standard
Supplement 28 Manufacturing (CMC) Approved July 27, 2007 N/A
Supplement 23 Labeling Approved March 24, 2003 Standard
Supplement 21 Labeling Approved January 10, 2002 Standard
Supplement 22 Manufacturing (CMC) Approved September 24, 2001 Standard
Supplement 20 Labeling Approved March 8, 2001 Standard
Supplement 19 Manufacturing (CMC) Approved March 8, 2001 Standard
Supplement 18 Manufacturing (CMC) Approved March 8, 2001 Standard
Supplement 17 Manufacturing (CMC) Approved October 25, 2000 Standard
Supplement 16 Manufacturing (CMC) Approved March 23, 2000 Standard
Supplement 15 Manufacturing (CMC) Approved March 1, 2000 Standard
Supplement 14 Manufacturing (CMC) Approved November 10, 1999 Standard
Supplement 13 Labeling Approved February 22, 1999 Standard
Supplement 11 Labeling Approved July 29, 1997 Standard
Supplement 12 Manufacturing (CMC) Approved July 10, 1997 Standard
Supplement 9 Labeling Approved February 22, 1996 Standard
Supplement 7 Labeling Approved August 23, 1994 Standard
Supplement 6 Labeling Approved August 9, 1994 —
Supplement 8 Manufacturing (CMC) Approved May 27, 1994 Standard
Supplement 5 Labeling Approved July 3, 1990 —
Supplement 4 Labeling Approved February 16, 1988 —
Supplement 3 Manufacturing (CMC) Approved January 29, 1987 Standard
Supplement 2 Labeling Approved September 19, 1986 —
Supplement 1 Manufacturing (CMC) Approved January 27, 1984 Standard
Original application 1 Type 5 - New Formulation or New Manufacturer Approved November 19, 1980 Standard

Review documents

  • 0 · Supplement · August 4, 2021
  • 0 · Supplement · May 12, 2021
  • 0 · Supplement · October 3, 2014
  • 0 · Supplement · October 3, 2014
  • 0 · Supplement · April 4, 2008
  • 0 · Supplement · April 4, 2008
  • 0 · Supplement · July 31, 2007
  • 0 · Supplement · July 30, 2007
  • 0 · Supplement · March 26, 2003
  • 0 · Supplement · January 10, 2002
  • 0 · Supplement · July 29, 1997

Prescribing information

Source: openFDA Drug Labeling

Reproduced verbatim from the Structured Product Labeling submitted to the FDA (effective 20260506). This is the manufacturer's labelling text, not a summary and not advice.

HUMAN PRESCRIPTION DRUG · 20260506 HUMAN PRESCRIPTION DRUG · 20260506

Boxed Warning

openFDA Drug Labeling

IMPORTANT NOTICE Elective induction of labor is defined as the initiation of labor in a pregnant individual who has no medical indications for induction. Since the available data are inadequate to evaluate the benefits-to-risks considerations, Pitocin is not indicated for elective induction of labor.

Indications and Usage

openFDA Drug Labeling

INDICATIONS AND USAGE IMPORTANT NOTICE Elective induction of labor is defined as the initiation of labor in a pregnant individual who has no medical indications for induction. Since the available data are inadequate to evaluate the benefits-to-risks considerations, Pitocin is not indicated for elective induction of labor. Antepartum: Pitocin is indicated for the initiation or improvement of uterine contractions, where this is desirable and considered suitable for reasons of fetal or maternal concern, in order to achieve vaginal delivery. It is indicated for (1) induction of labor in patients with a medical indication for the initiation of labor, such as Rh problems, maternal diabetes, preeclampsia at or near term, when delivery is in the best interests of mother and fetus or when membranes are prematurely ruptured and delivery is indicated; (2) stimulation or reinforcement of labor, as in selected cases of uterine inertia; (3) as adjunctive therapy in the management of incomplete or inevitable abortion. In the first trimester, curettage is generally considered primary therapy. In second trimester abortion, oxytocin infusion will often be successful in emptying the uterus. Other means of therapy, however, may be required in such cases. Postpartum: Pitocin is indicated to produce uterine contractions during the third stage of labor and to control postpartum bleeding or hemorrhage.

Dosage and Administration

openFDA Drug Labeling

DOSAGE AND ADMINISTRATION Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permit. The dosage of oxytocin is determined by the uterine response and must therefore be individualized and initiated at a very low level. The following dosage information is based upon various regimens and indications in general use. A. Induction or Stimulation of Labor Intravenous infusion (drip method) is the only acceptable method of parenteral administration of Pitocin for the induction or stimulation of labor. Accurate control of the rate of infusion is essential and is best accomplished by an infusion pump. It is convenient to piggyback the Pitocin infusion on a physiologic electrolyte solution, permitting the Pitocin infusion to be stopped abruptly without interrupting the electrolyte infusion. This is done in the following way. 1. Preparation a. The standard solution for infusion of Pitocin is prepared by adding 1 mL (containing 10 units of oxytocin) to 1000 mL of 0.9% aqueous sodium chloride or Ringer’s lactate. The combined solution containing 10 milliunits (mU) of oxytocin/mL is rotated in the infusion bottle for thorough mixing. b. Establish the infusion with a separate bottle of physiologic electrolyte solution not containing Pitocin. c. Attach (piggyback) the Pitocin-containing bottle with the infusion pump to the infusion line as close to the infusion site as possible. 2. Administration The initial dose should be 0.5–1 mU/min (equal to 3–6 mL of the dilute oxytocin solution per hour). At 30–60 minute intervals the dose should be gradually increased in increments of 1–2 mU/min until the desired contraction pattern has been established. Once the desired frequency of contractions has been reached and labor has progressed to 5–6 cm dilation, the dose may be reduced by similar increments. Studies of the concentrations of oxytocin in the maternal plasma during Pitocin infusion have shown that infusion rates up to 6 mU/min give the same oxytocin levels that are found in spontaneous labor. At term, higher infusion rates should be given with great care, and rates exceeding 9–10 mU/min are rarely required. Before term, when the sensitivity of the uterus is lower because of a lower concentration of oxytocin receptors, a higher infusion rate may be required. 3. Monitoring a. Electronically monitor the uterine activity and the fetal heart rate throughout the infusion of Pitocin. Attention should be given to tonus, amplitude and frequency of contractions, and to the fetal heart rate in relation to uterine contractions. If uterine contractions become too powerful, the infusion can be abruptly stopped, and oxytocic stimulation of the uterine musculature will soon wane (see PRECAUTIONS section). b. Discontinue the infusion of Pitocin immediately in the event of uterine hyperactivity and/or fetal distress. Administer oxygen to the mother, who preferably should be put in a lateral position. The condition of mother and fetus should immediately be evaluated by the responsible physician and appropriate steps taken. B. Control of Postpartum Uterine Bleeding Intravenous infusion (drip method). If the patient has an intravenous infusion running, 10 to 40 units of oxytocin may be added to the bottle, depending on the amount of electrolyte or dextrose solution remaining (maximum 40 units to 1000 mL). Adjust the infusion rate to sustain uterine contraction and control uterine atony. Intramuscular administration. 1 mL (10 units) of Pitocin can be given after the delivery of the placenta. C. Treatment of Incomplete, Inevitable, or Elective Abortion Intravenous infusion of 10 units of Pitocin added to 500 mL of a physiologic saline solution or 5% dextrose-in-water solution may help the uterus contract after a suction or sharp curettage for an incomplete, inevitable, or elective abortion. Subsequent to intra-amniotic injection of hypertonic saline, prostaglandins, ur …

Contraindications

openFDA Drug Labeling

CONTRAINDICATIONS Antepartum use of Pitocin is contraindicated in any of the following circumstances: Where there is significant cephalopelvic disproportion; In unfavorable fetal positions or presentations, such as transverse lies, which are undeliverable without conversion prior to delivery; In obstetrical emergencies where the benefit-to-risk ratio for either the fetus or the mother favors surgical intervention; In fetal distress where delivery is not imminent; Where adequate uterine activity fails to achieve satisfactory progress; Where the uterus is already hyperactive or hypertonic; In cases where vaginal delivery is contraindicated, such as invasive cervical carcinoma, active herpes genitalis, total placenta previa, vasa previa, and cord presentation or prolapse of the cord; In patients with hypersensitivity to the drug.

WARNINGS Pitocin, when given for induction of labor or augmentation of uterine activity, should be administered only by the intravenous route and with adequate medical supervision in a hospital.

Adverse Reactions

openFDA Drug Labeling

ADVERSE REACTIONS The following adverse reactions have been reported in the mother: Anaphylactic reaction Premature ventricular contractions Postpartum hemorrhage Pelvic hematoma Cardiac arrhythmia Subarachnoid hemorrhage Fatal afibrinogenemia Hypertensive episodes Nausea Rupture of the uterus Vomiting Excessive dosage or hypersensitivity to the drug may result in uterine hypertonicity, spasm, tetanic contraction, or rupture of the uterus. The possibility of increased blood loss and afibrinogenemia should be kept in mind when administering the drug. Severe water intoxication with convulsions and coma has occurred, associated with a slow oxytocin infusion over a 24-hour period. Maternal death due to oxytocin-induced water intoxication has been reported. The following adverse reactions have been reported in the fetus or neonate: Due to induced uterine motility: Due to use of oxytocin in the mother: Bradycardia Low Apgar scores at five minutes Premature ventricular contractions and other arrhythmias Neonatal jaundice Permanent CNS or brain damage Neonatal retinal hemorrhage Fetal death Neonatal seizures have been reported with the use of Pitocin. For medical advice about adverse reactions contact your medical professional. To report SUSPECTED ADVERSE REACTIONS, contact Par Health at 1-800-828-9393 or FDA at 1-800-FDA-1088 (1-800-332-1088) or www.fda.gov/medwatch .

Drug Interactions

openFDA Drug Labeling

Drug Interactions Severe hypertension has been reported when oxytocin was given three to four hours following prophylactic administration of a vasoconstrictor in conjunction with caudal block anesthesia. Cyclopropane anesthesia may modify oxytocin's cardiovascular effects, so as to produce unexpected results such as hypotension. Maternal sinus bradycardia with abnormal atrioventricular rhythms has also been noted when oxytocin was used concomitantly with cyclopropane anesthesia.

Description

openFDA Drug Labeling

DESCRIPTION Pitocin (oxytocin injection, USP) is a sterile, clear, colorless aqueous solution of synthetic oxytocin, for intravenous infusion or intramuscular injection. Pitocin is a nonapeptide found in pituitary extracts from mammals. It is standardized to contain 10 units of oxytocic hormone/mL and contains 0.5% Chlorobutanol, a chloroform derivative as a preservative, 1.65 mg acetic acid and 0.16 mg ammonium acetate as buffers, and with the pH adjusted with acetic acid to achieve a targeted pH of 3.5. Pitocin may contain up to 16% of total impurities. The hormone is prepared synthetically to avoid possible contamination with vasopressin (ADH) and other small polypeptides with biologic activity. Pitocin has the empirical formula C 43 H 66 N 12 O 12 S 2 (molecular weight 1007.19). The structural formula is as follows: Chemical Structure

OVERDOSAGE Overdosage with oxytocin depends essentially on uterine hyperactivity whether or not due to hypersensitivity to this agent. Hyperstimulation with strong (hypertonic) or prolonged (tetanic) contractions, or a resting tone of 15 to 20 mmHg or more between contractions can lead to tumultuous labor, uterine rupture, cervical and vaginal lacerations, postpartum hemorrhage, uteroplacental hypoperfusion, and variable deceleration of fetal heart, fetal hypoxia, hypercapnia, perinatal hepatic necrosis or death. Water intoxication with convulsions, which is caused by the inherent antidiuretic effect of oxytocin, is a serious complication that may occur if large doses (40 to 50 milliunits/minute) are infused for long periods. Management consists of immediate discontinuation of oxytocin and symptomatic and supportive therapy.

How Supplied / Storage and Handling

openFDA Drug Labeling

HOW SUPPLIED Pitocin (Oxytocin Injection, USP) Synthetic is available as follows: NDC 42023-116-25 Packages of twenty-five oversized 1-mL single-dose vials, each containing 10 units of oxytocin. NDC 42023-116-02 Packages of twenty-five 10 mL multiple-dose vial, each containing 10 units of oxytocin per mL (total = 100 units of oxytocin per vial). STORAGE Store between 20° to 25°C (68° to 77°F). (See USP Controlled Room Temperature.)

Adverse event reports

Source: openFDA FAERS
2,984
FAERS reports mentioning this drug
as of 2026-09-25T03:42:24+00:00
A report count is not a risk measure. FAERS accepts voluntary and mandatory reports without establishing causation, and reporting is influenced by how widely a drug is used, how long it has been marketed, and media attention. FDA states that reports “do not prove that the drug caused the event”. Compare rates, not totals.

Attributed to this product's most-reported active ingredient: OXYTOCIN. Combination products with more than six active ingredients are not attributed, because a report count summed across a long ingredient list measures the list, not the medicine.

Recalls

Source: FDA Enforcement
Drug recall enforcement reports associated with this product.
Classification Reported Firm Reason Status
Class III July 25, 2012 JHP Pharmaceuticals, LLC Labeling: Label Mix-up: Pitocin storage conditions should be labeled, "Store between 20¿ to 25¿C (68¿ to 77¿F)". Pitocin lot 225867 and part of Pitocin lot 231423 were labeled, "Store between 20¿ to 25¿C (28¿ to 77¿F)". Terminated

Packaging and NDCs

Source: NDC Directory
Every National Drug Code package associated with this medication. The NDC is the identifier used for dispensing, billing and pharmacovigilance in the United States.
Package NDC Product NDC Labeler Description Marketing start
42023-116-02 42023-116 Par Health USA, LLC 25 VIAL in 1 CARTON (42023-116-02) / 10 mL in 1 VIAL February 1, 2008
42023-116-25 42023-116 Par Health USA, LLC 25 VIAL in 1 TRAY (42023-116-25) / 1 mL in 1 VIAL February 1, 2008
42023-116-73 42023-116 Par Health USA, LLC 25 VIAL in 1 CARTON (42023-116-73) / 10 mL in 1 VIAL December 22, 2023
42023-116-83 42023-116 Par Health USA, LLC 25 VIAL in 1 CARTON (42023-116-83) / 1 mL in 1 VIAL December 22, 2023
42023-116-93 42023-116 Par Health USA, LLC 25 VIAL in 1 CARTON (42023-116-93) / 10 mL in 1 VIAL May 6, 2024
42023-130-06 42023-130 Par Health USA, LLC 6 VIAL in 1 CARTON (42023-130-06) / 50 mL in 1 VIAL May 1, 2018
42023-116 42023-116 Par Health USA, LLC — May 6, 2024
42023-130 42023-130 Par Health USA, LLC — May 1, 2018

Sources for this page

Every dataset that contributed a fact to this page.
Dataset Agency Used for
NDC Directory FDA Identity, ingredients, strengths, forms, routes, labelers, packages
Drugs@FDA FDA Application, sponsor, submissions, review documents, marketing status
Orange Book FDA Therapeutic equivalence codes, reference drug flags, patents, exclusivity
Drug Labeling FDA / NLM Prescribing information reproduced above
FAERS FDA Adverse event report counts
Enforcement FDA Recall records

Generated September 25, 2026 · 12 sections on this page.