NDC 65862-557 – Minocycline Hydrochloride

Minocycline Hydrochloride 115 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC65862-557

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
September 28, 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 (2)

Package NDCDescriptionSince
65862-557-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-557-30)Sep 28, 2018
65862-557-991000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-557-99)Sep 28, 2018

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