Glimepiride

Product NDC

69452-129

11-digit product format

694520129

Labeler code

69452

Product ID

69452-129_f7511fbc-d31b-4338-9109-a774bba0d4f6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glimepiride

Dosage form

TABLET

Route

ORAL

Labeler

Bionpharma Inc.

Application

ANDA091220

Marketing category

ANDA

Marketing start

2015-10-01

Marketing end

2020-02-29

Substance

GLIMEPIRIDE

Active strength

2 mg/1

Pharmacologic classes

Sulfonylurea [EPC],Sulfonylurea Compounds [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record