Propranolol Hydrochloride

Product NDC

50436-0902

11-digit product format

504360902

Labeler code

50436

Product ID

50436-0902_2b391cef-e0c3-48d4-8d53-a6bd95e841e7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

propranolol hydrochloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

Unit Dose Services

Application

NDA018553

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2009-02-25

Marketing end

0000-00-00

Substance

PROPRANOLOL HYDROCHLORIDE

Active strength

120 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