NDC 68382-532 – Minocycline hydrochloride

Minocycline Hydrochloride 65 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC68382-532

Product details

Brand name
Minocycline hydrochloride
Generic name
Minocycline hydrochloride
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA203553
Marketed since
June 12, 2025
Listing expires
December 31, 2026
Pharmacologic class
Tetracycline-class Drug

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
68382-532-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-532-01)Jun 12, 2025
68382-532-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-532-05)Jun 12, 2025
68382-532-0630 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-532-06)Jun 12, 2025
68382-532-101000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-532-10)Jun 12, 2025
68382-532-1690 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-532-16)Jun 12, 2025
68382-532-3010 BLISTER PACK in 1 CARTON (68382-532-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACKJun 12, 2025

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