Glimepiride

Product NDC

35356-896

11-digit product format

353560896

Labeler code

35356

Product ID

35356-896_ff87b26f-fd4c-46a0-a3f9-3b7704a4af01

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glimepiride

Dosage form

TABLET

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA077091

Marketing category

ANDA

Marketing start

2005-10-06

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

2019-12-31

Current FDA listing

Historical FDA.report record