NDC 68382-535 – Minocycline hydrochloride

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

Human Prescription Drug

Product NDC68382-535

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
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
68382-535-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-535-01)Mar 7, 2018
68382-535-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-535-05)Mar 7, 2018
68382-535-0630 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-535-06)Mar 7, 2018
68382-535-101000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-535-10)Mar 7, 2018
68382-535-1690 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-535-16)Mar 7, 2018
68382-535-3010 BLISTER PACK in 1 CARTON (68382-535-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMar 7, 2018

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