Propranolol Hydrochloride

Product NDC

70518-1286

11-digit product format

705181286

Labeler code

70518

Product ID

70518-1286_912a1379-de79-f1cd-e053-2a95a90a3a9c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

propranolol hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA070213

Marketing category

ANDA

Marketing start

2018-07-09

Marketing end

0000-00-00

Substance

PROPRANOLOL HYDROCHLORIDE

Active strength

10 mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record