Propranolol Hydrochloride

Product NDC

50090-2869

11-digit product format

500902869

Labeler code

50090

Product ID

50090-2869_97e597e4-284e-4207-b922-a10d4e9fa8d3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Propranolol Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA078955

Marketing category

ANDA

Marketing start

2008-10-13

Marketing end

0000-00-00

Substance

PROPRANOLOL HYDROCHLORIDE

Active strength

40 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