Glimepiride

Product NDC

68071-1991

11-digit product format

680711991

Labeler code

68071

Product ID

68071-1991_490f2701-bf79-07ec-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glimepiride

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA091220

Marketing category

ANDA

Marketing start

2015-10-01

Marketing end

0000-00-00

Substance

GLIMEPIRIDE

Active strength

1 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