Naloxone — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

NALOXONE HYDROCHLORIDE DIHYDRATE

Base moiety

NALOXONE

RxNorm CUI

351267

UNII

56W8MW3EN1

Medication products

8

Brand names

3

Dosage forms

3

FAERS reports

124,274 · not a risk measure

Products containing this ingredient

Source: NDC Directory 8 products

Naloxone Powder
1 NDC
Naloxone HCl Dihydrate Powder
1 NDC
NALOXONE HYDROCHLORIDE Naloxone Hydrochloride · Powder
10 NDC
Naloxone Hydrochloride Dihydrate Powder
6 NDC
Buprenorphine and Naloxone Tablet
Rx ANDA TE AB 1 recall 29 NDC
Buprenorphine and Naloxone Film
Rx ANDA TE AB 1 recall 19 NDC
Buprenorphine HCl and Naloxone HCl Buprenorphine and Naloxone · Tablet
Rx ANDA TE AB 7 NDC
buprenorphine hydrochloride and naloxone hydrochloride dihydrate Tablet
Rx ANDA TE AB 23 NDC

Entries without a link are products listed by the FDA that carry no approval record, therapeutic equivalence rating or official labelling, so they have no detail page. Their facts are shown inline.

By dosage form

How this ingredient is presented across the catalogue.
Dosage form	Products	Examples
Powder	4	Naloxone, Naloxone HCl Dihydrate, NALOXONE HYDROCHLORIDE, Naloxone Hydrochloride Dihydrate
Tablet	3	Buprenorphine and Naloxone, Buprenorphine HCl and Naloxone HCl, buprenorphine hydrochloride and naloxone hydrochloride dihydrate
Film	1	Buprenorphine and Naloxone

Sources for this page

Dataset	Agency	Used for
NDC Directory	FDA	Ingredient name, strengths, products, labelers, packages
DailyMed RxNorm mappings	NLM	RxNorm concept identifier (RxCUI)
FAERS	FDA	Adverse event report totals