Propranolol Hydrochloride

Product NDC

63629-2570

11-digit product format

636292570

Labeler code

63629

Product ID

63629-2570_f8af56d5-a474-4c69-94a7-4b8f7f6ad536

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Propranolol Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA078955

Marketing category

ANDA

Marketing start

2008-10-13

Marketing end

0000-00-00

Substance

PROPRANOLOL HYDROCHLORIDE

Active strength

20 mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record