Propranolol Hydrochloride

Product NDC

50436-4313

11-digit product format

504364313

Labeler code

50436

Product ID

50436-4313_c9c3ac59-f1d5-4f0c-9f84-f34b1fecf258

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Propranolol Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record