NDC 65862-556 – Minocycline Hydrochloride

Minocycline Hydrochloride 90 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC65862-556

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
November 19, 2012
Listing expires
December 31, 2026
Pharmacologic class
Tetracycline-class Drug

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
65862-556-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-556-01)Nov 19, 2012
65862-556-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-556-30)Nov 19, 2012
65862-556-991000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-556-99)Nov 19, 2012

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