NDC 70771-1167 – Minocycline hydrochloride

Minocycline Hydrochloride 135 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC70771-1167

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
March 7, 2018
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
70771-1167-01000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1167-0)Mar 7, 2018
70771-1167-1100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1167-1)Mar 7, 2018
70771-1167-330 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1167-3)Mar 7, 2018
70771-1167-5500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1167-5)Mar 7, 2018
70771-1167-710 BLISTER PACK in 1 CARTON (70771-1167-7) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMar 7, 2018
70771-1167-990 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1167-9)Mar 7, 2018

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