Minocycline — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

MINOCYCLINE HYDROCHLORIDE

Base moiety

MINOCYCLINE

RxNorm CUI

197985

UNII

0020414E5U

Medication products

13

Brand names

7

Dosage forms

8

FAERS reports

5,809 · not a risk measure

Products containing this ingredient

Source: NDC Directory 13 products

AMZEEQ Minocycline · Aerosol, Foam
Rx NDA 1 NDC
Arestin Minocycline Hydrochloride · Powder
Rx NDA 1 NDC
EMROSI Minocycline Hydrochloride Extended-Release · Capsule
Rx NDA 1 NDC
Minocin minocycline hydrochloride · Injection
Rx NDA TE AP 1 NDC
MINOCYCLINE Minocycline · Powder
1 NDC
Minocycline HCl Powder
2 NDC
Minocycline Hydrochloride Powder
8 NDC
ZILXI Minocycline · Aerosol, Foam
Rx NDA 1 NDC
Minocycline Hydrochloride Capsule
Rx ANDA TE AB 50 NDC
Minocycline Hydrochloride Tablet, Film Coated, Extended Release
Rx ANDA TE AB 2 recalls 44 NDC
Minocycline Hydrochloride Tablet
Rx ANDA TE AB 10 NDC
minocycline hydrochloride Tablet, Extended Release
Rx ANDA TE AB 20 NDC
Minocycline Hydrochloride Tablet, Film Coated
ANDA TE AB 3 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	Arestin, MINOCYCLINE, Minocycline HCl, Minocycline Hydrochloride
AEROSOL, Foam	2	AMZEEQ, ZILXI
Capsule	2	EMROSI, Minocycline Hydrochloride
Injection	1	Minocin
TABLET, Film COATED, Extended Release	1	Minocycline Hydrochloride
Tablet	1	Minocycline Hydrochloride
TABLET, Extended Release	1	minocycline hydrochloride
TABLET, Film Coated	1	Minocycline Hydrochloride

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