Propranolol Hydrochloride

Product NDC

63629-7176

11-digit product format

636297176

Labeler code

63629

Product ID

63629-7176_c04039e6-f053-4aac-8eb6-7e4a9e9fee34

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

propranolol hydrochloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

Bryant Ranch Prepack

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