NDC 59651-338 – Minocycline Hydrochloride

Minocycline Hydrochloride 75 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC59651-338

Product details

Brand name
Minocycline Hydrochloride
Generic name
Minocycline Hydrochloride
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213662
Marketed since
May 1, 2020
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
59651-338-01100 TABLET, FILM COATED in 1 CONTAINER (59651-338-01)May 1, 2020

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