NDC 70771-1153 – Minocycline hydrochloride

Minocycline Hydrochloride 55 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC70771-1153

Product details

Brand name
Minocycline hydrochloride
Generic name
Minocycline hydrochloride
Labeler
Zydus Lifesciences Limited
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
70771-1153-01000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-0)Jun 12, 2025
70771-1153-1100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-1)Jun 12, 2025
70771-1153-330 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-3)Jun 12, 2025
70771-1153-5500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-5)Jun 12, 2025
70771-1153-710 BLISTER PACK in 1 CARTON (70771-1153-7) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACKJun 12, 2025
70771-1153-990 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-9)Jun 12, 2025

Other Minocycline Hydrochloride products