Glipizide and Metformin Hydrochloride

Product NDC

70518-0116

11-digit product format

705180116

Labeler code

70518

Product ID

70518-0116_81dc5dbd-184e-134f-e053-2991aa0a75ee

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

glipizide and metformin hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA078083

Marketing category

ANDA

Marketing start

2017-01-12

Marketing end

0000-00-00

Substance

GLIPIZIDE; METFORMIN HYDROCHLORIDE

Active strength

5 mg/1; mg/1

Pharmacologic classes

Sulfonylurea [EPC],Sulfonylurea Compounds [CS],Biguanide [EPC],Biguanides [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record