Benzphetamine Hydrochloride

Product NDC

71335-0768

11-digit product format

713350768

Labeler code

71335

Product ID

71335-0768_6c74ee41-01cb-4653-97c9-430ffad35e14

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benzphetamine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA040747

Marketing category

ANDA

Marketing start

2016-01-15

Marketing end

0000-00-00

Substance

BENZPHETAMINE HYDROCHLORIDE

Active strength

50 mg/1

Pharmacologic classes

Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]

DEA schedule

CIII

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record