Repaglinide

Product NDC

51079-539

11-digit product format

510790539

Labeler code

51079

Product ID

51079-539_7d7c90ae-ab87-0bc2-e053-2991aa0a6602

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

repaglinide

Dosage form

TABLET

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA090252

Marketing category

ANDA

Marketing start

2014-02-27

Marketing end

2019-03-31

Substance

REPAGLINIDE

Active strength

1 mg/1

Pharmacologic classes

Glinide [EPC],P

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record