NDC 65862-884 – Minocycline Hydrochloride

Minocycline Hydrochloride 80 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC65862-884

Product details

Brand name
Minocycline Hydrochloride
Generic name
Minocycline Hydrochloride
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA202261
Marketed since
June 13, 2016
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
65862-884-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-884-01)Jun 13, 2016
65862-884-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-884-05)Jun 13, 2016
65862-884-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-884-30)Jun 13, 2016
65862-884-991000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-884-99)Jun 13, 2016

Other Minocycline Hydrochloride products