NDC 71335-0682 – Minocycline Hydrochloride

Minocycline Hydrochloride 50 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-0682

Product details

Brand name
Minocycline Hydrochloride
Generic name
Minocycline Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA063181
Marketed since
February 1, 1992
Listing expires
December 31, 2026
Pharmacologic class
Tetracycline-class Drug

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
71335-0682-190 CAPSULE in 1 BOTTLE (71335-0682-1)Sep 17, 2015
71335-0682-250 CAPSULE in 1 BOTTLE (71335-0682-2)Sep 17, 2015
71335-0682-360 CAPSULE in 1 BOTTLE (71335-0682-3)Sep 17, 2015
71335-0682-430 CAPSULE in 1 BOTTLE (71335-0682-4)Sep 17, 2015
71335-0682-5100 CAPSULE in 1 BOTTLE (71335-0682-5)Sep 17, 2015

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