Propranolol Hydrochloride

Product NDC

70518-1963

11-digit product format

705181963

Labeler code

70518

Product ID

70518-1963_84688910-247b-56e3-e053-2a91aa0a473a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

propranolol hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA070213

Marketing category

ANDA

Marketing start

2019-03-18

Marketing end

0000-00-00

Substance

PROPRANOLOL HYDROCHLORIDE

Active strength

20 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