NDC 68180-379 – Minocycline Hydrochloride

Minocycline Hydrochloride 45 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC68180-379

Product details

Brand name
Minocycline Hydrochloride
Generic name
Minocycline Hydrochloride
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA091424
Marketed since
February 14, 2012
Listing expires
December 31, 2026
Pharmacologic class
Tetracycline-class Drug

Active ingredients

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

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