Repaglinide

Product NDC

68084-967

11-digit product format

680840967

Labeler code

68084

Product ID

68084-967_9f0728eb-a746-23bd-e053-2995a90aea9e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Repaglinide

Dosage form

TABLET

Route

ORAL

Labeler

American Health Packaging

Application

ANDA077571

Marketing category

ANDA

Marketing start

2015-08-24

Marketing end

2020-12-31

Substance

REPAGLINIDE

Active strength

2 mg/1

Pharmacologic classes

Glinide [EPC],Potassium Channel Antagonists [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record