Glimepiride

Product NDC

70518-0907

11-digit product format

705180907

Labeler code

70518

Product ID

70518-0907_8f08ecc1-5b44-186e-e053-2a95a90a55fe

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glimepiride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077911

Marketing category

ANDA

Marketing start

2017-12-13

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