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Buprenorphine

Active ingredient 7 prescription 30 with labelling

Overview

Source: NDC Directory

Ingredient name

BUPRENORPHINE

Base moiety

BUPRENORPHINE

RxNorm CUI

904870

UNII

40D3SCR4GZ

Medication products

Brand names

Dosage forms

FAERS reports

124,274 · not a risk measure

Products containing this ingredient

Source: NDC Directory 9 products

Buprenorphine Powder
15 NDC
Buprenorphine Base Powder
3 NDC
BRIXADI Buprenorphine · Injection
Rx NDA 7 NDC
Buprenorphine Patch, Extended Release
Rx ANDA TE AB 1 recall 20 NDC
Buprenorphine Patch
Rx NDA TE AB 5 NDC
Buprenorphine and Naloxone Tablet
Rx ANDA TE AB 1 recall 29 NDC
buprenorphine transdermal system buprenorphine · Patch, Extended Release
Rx ANDA TE AB 5 NDC
Butrans buprenorphine · Patch, Extended Release
Rx NDA TE AB 5 NDC
SUBLOCADE buprenorphine · Solution
Rx NDA 2 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
PATCH, Extended Release	3	Buprenorphine, buprenorphine transdermal system, Butrans
Powder	2	Buprenorphine, Buprenorphine Base
Injection	1	BRIXADI
Patch	1	Buprenorphine
Tablet	1	Buprenorphine and Naloxone
Solution	1	SUBLOCADE

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