NDC 67877-436 – Minocycline Hydrochloride

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

Human Prescription Drug 2 recalls

Product NDC67877-436

Product details

Brand name
Minocycline Hydrochloride
Generic name
Minocycline Hydrochloride
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA204453
Marketed since
December 23, 2019
Listing expires
December 31, 2026
Pharmacologic class
Tetracycline-class Drug

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
67877-436-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-436-01)Dec 23, 2019
67877-436-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-436-05)Dec 23, 2019
67877-436-1410 BLISTER PACK in 1 CARTON (67877-436-14) / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKDec 23, 2019
67877-436-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-436-30)Dec 23, 2019

Recalls mentioning this NDC

Other Minocycline Hydrochloride products