Glimepiride

Product NDC

50090-3172

11-digit product format

500903172

Labeler code

50090

Product ID

50090-3172_70f064a7-147a-4f34-8a12-bb482512d28e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glimepiride

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA202112

Marketing category

ANDA

Marketing start

2015-07-14

Marketing end

0000-00-00

Substance

GLIMEPIRIDE

Active strength

4 mg/1

Pharmacologic classes

Sulfonylurea [EPC],Sulfonylurea Compounds [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record