NDC 42806-081 – Benzphetamine Hydrochloride

Benzphetamine Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CIII

Product NDC42806-081

Product details

Brand name
Benzphetamine Hydrochloride
Generic name
Benzphetamine Hydrochloride
Labeler
Epic Pharma, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090346
Marketed since
December 16, 2015
Listing expires
December 31, 2026
Pharmacologic class
Sympathomimetic Amine Anorectic

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
42806-081-01100 TABLET, FILM COATED in 1 BOTTLE (42806-081-01)Dec 16, 2015
42806-081-05500 TABLET, FILM COATED in 1 BOTTLE (42806-081-05)Dec 16, 2015
42806-081-3030 TABLET, FILM COATED in 1 BOTTLE (42806-081-30)Dec 16, 2015

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