NDC 62135-889 – Minocycline Hydrochloride

Minocycline Hydrochloride 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC62135-889

Product details

Brand name
Minocycline Hydrochloride
Generic name
Minocycline Hydrochloride
Labeler
Chartwell RX, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA065436
Marketed since
December 26, 2007
Listing expires
December 31, 2026
Pharmacologic class
Tetracycline-class Drug

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
62135-889-6060 TABLET in 1 BOTTLE (62135-889-60)Jun 13, 2025

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