NDC 71335-1045 – Minocycline Hydrochloride

Minocycline Hydrochloride 100 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-1045

Product details

Brand name
Minocycline Hydrochloride
Generic name
Minocycline Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA063065
Marketed since
May 1, 1993
Listing expires
December 31, 2026
Pharmacologic class
Tetracycline-class Drug

Active ingredients

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

Package NDC codes (10)

Package NDCDescriptionSince
71335-1045-050 CAPSULE in 1 BOTTLE (71335-1045-0)Jan 14, 2019
71335-1045-120 CAPSULE in 1 BOTTLE (71335-1045-1)Jan 14, 2019
71335-1045-230 CAPSULE in 1 BOTTLE (71335-1045-2)Jan 14, 2019
71335-1045-328 CAPSULE in 1 BOTTLE (71335-1045-3)Jan 14, 2019
71335-1045-460 CAPSULE in 1 BOTTLE (71335-1045-4)Jan 14, 2019
71335-1045-5100 CAPSULE in 1 BOTTLE (71335-1045-5)Jan 14, 2019
71335-1045-614 CAPSULE in 1 BOTTLE (71335-1045-6)Jan 14, 2019
71335-1045-7120 CAPSULE in 1 BOTTLE (71335-1045-7)Jan 14, 2019
71335-1045-890 CAPSULE in 1 BOTTLE (71335-1045-8)Jan 14, 2019
71335-1045-915 CAPSULE in 1 BOTTLE (71335-1045-9)Jan 14, 2019

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