Metoprolol Succinate

Product NDC

70518-0611

11-digit product format

705180611

Labeler code

70518

Product ID

70518-0611_a50c0b9b-af65-40ec-e053-2a95a90a435d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metoprolol Succinate

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077298

Marketing category

ANDA

Marketing start

2017-07-07

Marketing end

0000-00-00

Substance

METOPROLOL SUCCINATE

Active strength

100 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record