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FDA ANDA · ANDA090867

MINOCYCLINE HYDROCHLORIDE

Sponsor: SUN PHARM INDS INC

APPLICATION
ANDA090867
TYPE
ANDA
ORIGINAL APPROVAL
2013-05-13
LATEST ACTION
2013-07-18
ROUTE
ORAL
DOSAGE FORM
CAPSULE
MARKETING STATUS
Discontinued

Products

MINOCYCLINE HYDROCHLORIDEDiscontinued
MINOCYCLINE HYDROCHLORIDE EQ 100MG BASE · CAPSULE · ORAL
MINOCYCLINE HYDROCHLORIDEDiscontinued
MINOCYCLINE HYDROCHLORIDE EQ 50MG BASE · CAPSULE · ORAL
MINOCYCLINE HYDROCHLORIDEDiscontinued
MINOCYCLINE HYDROCHLORIDE EQ 75MG BASE · CAPSULE · ORAL

Approval history

2013-07-18Labeling · Supplement 1 · standardAP
2013-05-13OriginalAP
VIEW ON DRUGS@FDA ↗

Related on SPEQ

Pharma industry →GMP discipline →FDA drug shortages →FDA enforcement & recalls →

Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

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