Metoprolol Tartrate

Product NDC

68071-4571

11-digit product format

680714571

Labeler code

68071

Product ID

68071-4571_7666e252-c1ab-6500-e053-2991aa0aa970

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metoprolol Tartrate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA200981

Marketing category

ANDA

Marketing start

2015-08-14

Marketing end

0000-00-00

Substance

METOPROLOL TARTRATE

Active strength

25 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