NDC 71335-0451 – Benzphetamine Hydrochloride

Benzphetamine Hydrochloride 50 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIII

Product NDC71335-0451

Product details

Brand name
Benzphetamine Hydrochloride
Generic name
benzphetamine hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090968
Marketed since
July 21, 2010
Listing expires
December 31, 2026
Pharmacologic class
Sympathomimetic Amine Anorectic

Active ingredients

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

Package NDC codes (9)

Package NDCDescriptionSince
71335-0451-130 TABLET in 1 BOTTLE (71335-0451-1)Aug 17, 2018
71335-0451-27 TABLET in 1 BOTTLE (71335-0451-2)Jul 25, 2018
71335-0451-314 TABLET in 1 BOTTLE (71335-0451-3)Jul 25, 2018
71335-0451-421 TABLET in 1 BOTTLE (71335-0451-4)Sep 14, 2018
71335-0451-542 TABLET in 1 BOTTLE (71335-0451-5)Apr 23, 2018
71335-0451-684 TABLET in 1 BOTTLE (71335-0451-6)May 29, 2024
71335-0451-760 TABLET in 1 BOTTLE (71335-0451-7)Jul 10, 2018
71335-0451-890 TABLET in 1 BOTTLE (71335-0451-8)Feb 12, 2018
71335-0451-9120 TABLET in 1 BOTTLE (71335-0451-9)May 29, 2018

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