Propranolol Hydrochloride

Product NDC

43478-902

11-digit product format

434780902

Labeler code

43478

Product ID

43478-902_54753570-5982-418f-acea-aabf39c8a50b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

propranolol hydrochloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

Rouses Point Pharm

Application

NDA018553

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2009-02-25

Marketing end

2019-07-31

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

0000-00-00

Current FDA listing

Historical FDA.report record