NDC 72162-2575 – Minocycline Hydrochloride

Minocycline Hydrochloride 50 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72162-2575

Product details

Brand name
Minocycline Hydrochloride
Generic name
Minocycline Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA065156
Marketed since
April 2, 2015
Listing expires
December 31, 2027
Pharmacologic class
Tetracycline-class Drug

Active ingredients

Uses, dosage, side effects and warnings for Minocycline Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
72162-2575-1100 TABLET in 1 BOTTLE (72162-2575-1)Nov 17, 2025

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