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CLOTRIMAZOLE

Prescription ANDA TE AB 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
Clotrimazole
Generic name
Clotrimazole
Dosage form
Lozenge
Route
Oral
Marketing category
ANDA · ANDA
Labeler
Rising Pharma Holdings, Inc.
Product type
Human Prescription Drug
DEA schedule
Not scheduled
Active ingredients
1
NDC product codes
3
Packages
7
Data completeness
76% of corroborating sources present

Active ingredients

Source: NDC Directory
Active ingredients and strengths as listed in the NDC Directory.
Ingredient Strength RxCUI Monograph
Clotrimazole 10 mg/1 308714 View

Forms, strengths and routes

Source: NDC Directory
Dosage form
Lozenge
Route of administration
Oral
Presentations
10

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
Azole Antifungal [EPC] EPC All 44 members
Azoles [CS] CS All 44 members

Regulatory status

Source: Drugs@FDANDC Directory
Application number
215641
Application type
ANDA · Abbreviated New Drug Application
Approval date
February 29, 2024
Sponsor
THINQ PHARM-CRO PVT
Products on application
1
Submissions recorded
1
Products approved under application 215641.
Product Trade name Form Strength Ingredient Status TE Flags
215641-001 CLOTRIMAZOLE TROCHE/LOZENGE CLOTRIMAZOLE Prescription AB

Therapeutic equivalence

Source: Orange Book
TE code
AB
Reference Listed Drug
No
Reference Standard
No

What this rating means: Therapeutically equivalent — bioequivalence demonstrated by in vivo or in vitro testing

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 215641.
Type No. Action Status Date Review
Original application 1 Approved February 29, 2024 Standard

Prescribing information

Source: openFDA Drug Labeling

Reproduced verbatim from the Structured Product Labeling submitted to the FDA (effective 20250327). This is the manufacturer's labelling text, not a summary and not advice.

HUMAN PRESCRIPTION DRUG · 20250327 HUMAN PRESCRIPTION DRUG · 20210730

Indications and Usage

openFDA Drug Labeling

INDICATIONS AND USAGE Clotrimazole Lozenges are indicated for the local treatment of oropharyngeal candidiasis. The diagnosis should be confirmed by a KOH smear and/or culture prior to treatment. Clotrimazole Lozenges are also indicated prophylactically to reduce the incidence of oropharyngeal candidiasis in patients immunocompromised by conditions that include chemotherapy, radiotherapy, or steroid therapy utilized in the treatment of leukemia, solid tumors, or renal transplantation. There are no data from adequate and well-controlled trials to establish the safety and efficacy of this product for prophylactic use in patients immunocompromised by etiologies other than those listed in the previous sentence. (See DOSAGE AND ADMINISTRATION .)

Dosage and Administration

openFDA Drug Labeling

DOSAGE AND ADMINISTRATION Clotrimazole Lozenges are administered only as a lozenge that must be slowly dissolved in the mouth. The recommended dose is one lozenge five times a day for fourteen consecutive days. Only limited data are available on the safety and effectiveness of the clotrimazole lozenge after prolonged administration; therefore, therapy should be limited to short term use, if possible. For prophylaxis to reduce the incidence of oropharyngeal candidiasis in patients immunocompromised by conditions that include chemotherapy, radiotherapy, or steroid therapy utilized in the treatment of leukemia, solid tumors, or renal transplantation, the recommended dose is one lozenge three times daily for the duration of chemotherapy or until steroids are reduced to maintenance levels.

Contraindications

openFDA Drug Labeling

CONTRAINDICATIONS Clotrimazole Lozenges are contraindicated in patients who are hypersensitive to any of its components.

WARNING Clotrimazole Lozenges are not indicated for the treatment of systemic mycoses including systemic candidiasis.

Adverse Reactions

openFDA Drug Labeling

ADVERSE REACTIONS Abnormal liver function tests have been reported in patients treated with clotrimazole lozenges; elevated SGOT levels were reported in about 15% of patients in the clinical trials (See PRECAUTIONS ). Nausea, vomiting, unpleasant mouth sensations and pruritus have also been reported with the use of the lozenge. To report SUSPECTED ADVERSE REACTIONS, contact Rising Pharma Holdings, Inc. at 1-844-874-7464 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch

Description

openFDA Drug Labeling

DESCRIPTION Each Clotrimazole lozenge USP contains 10 mg clotrimazole USP [1-(o-chloro-α,α-diphenylbenzyl) imidazole], a synthetic antifungal agent, for topical use in the mouth. Structural Formula: Chemical Formula: C 22 H 17 ClN 2 The lozenge dosage form is a large, slowly dissolving lozenge containing 10 mg of clotrimazole USP dispersed in croscarmellose sodium, dextrates, magnesium stearate, microcrystalline cellulose and povidone. clotrimazole-structure.jpg

OVERDOSAGE No data available.

How Supplied / Storage and Handling

openFDA Drug Labeling

HOW SUPPLIED Clotrimazole Troche (lozenges) USP 10 mg troche is supplied as white, round, flat face beveled edge troche with product identification “54 552” on one side and plain on the other side. NDC 0054-4146-22: Bottle of 70 Troches NDC 0054-4146-23: Bottle of 140 Troches NDC 0054-8146-22: 7x10 Unit-Dose Troches Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room Temperature.] Avoid freezing. Distributed by: Hikma Pharmaceuticals USA Inc. Berkeley Heights, NJ 07922 C50000435/01 Revised July 2021

Adverse event reports

Source: openFDA FAERS
12,736
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: CLOTRIMAZOLE. 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.

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
0054-4146-22 0054-4146 Hikma Pharmacuticals USA USA Inc. 70 LOZENGE in 1 BOTTLE, PLASTIC (0054-4146-22) July 29, 2004
0054-4146-23 0054-4146 Hikma Pharmacuticals USA USA Inc. 140 LOZENGE in 1 BOTTLE, PLASTIC (0054-4146-23) July 29, 2004
0574-0107-14 0574-0107 Padagis US LLC 140 LOZENGE in 1 BOTTLE, PLASTIC (0574-0107-14) December 1, 2005
0574-0107-70 0574-0107 Padagis US LLC 70 LOZENGE in 1 BOTTLE, PLASTIC (0574-0107-70) December 1, 2005
0574-0107-77 0574-0107 Padagis US LLC 70 PACKET in 1 BOX (0574-0107-77) / 1 LOZENGE in 1 PACKET December 1, 2005
16571-686-07 16571-686 Rising Pharma Holdings, Inc. 70 LOZENGE in 1 BOTTLE (16571-686-07) May 1, 2024
16571-686-14 16571-686 Rising Pharma Holdings, Inc. 140 LOZENGE in 1 BOTTLE (16571-686-14) May 1, 2024
0054-4146 0054-4146 Hikma Pharmacuticals USA USA Inc. — July 29, 2004
0574-0107 0574-0107 Padagis US LLC — December 1, 2005
16571-686 16571-686 Rising Pharma Holdings, Inc. — May 1, 2024

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

Generated September 25, 2026 · 11 sections on this page.