NDC 71335-0046 – Minocycline Hydrochloride

Minocycline Hydrochloride 100 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-0046

Product details

Brand name
Minocycline Hydrochloride
Generic name
Minocycline Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA065062
Marketed since
April 2, 2015
Listing expires
December 31, 2027
Pharmacologic class
Tetracycline-class Drug

Active ingredients

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

Package NDC codes (10)

Package NDCDescriptionSince
71335-0046-050 CAPSULE in 1 BOTTLE (71335-0046-0)Apr 11, 2024
71335-0046-120 CAPSULE in 1 BOTTLE (71335-0046-1)Jun 19, 2018
71335-0046-230 CAPSULE in 1 BOTTLE (71335-0046-2)May 7, 2018
71335-0046-328 CAPSULE in 1 BOTTLE (71335-0046-3)Sep 5, 2024
71335-0046-460 CAPSULE in 1 BOTTLE (71335-0046-4)May 13, 2020
71335-0046-5100 CAPSULE in 1 BOTTLE (71335-0046-5)Sep 5, 2024
71335-0046-614 CAPSULE in 1 BOTTLE (71335-0046-6)Oct 1, 2018
71335-0046-7120 CAPSULE in 1 BOTTLE (71335-0046-7)Sep 5, 2024
71335-0046-890 CAPSULE in 1 BOTTLE (71335-0046-8)Apr 27, 2018
71335-0046-915 CAPSULE in 1 BOTTLE (71335-0046-9)Sep 5, 2024

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