Metformin Hydrochloride

Product NDC

0093-7212

11-digit product format

000937212

Labeler code

0093

Product ID

0093-7212_a84b54af-b795-44bf-bb70-ab9d029ec0c7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metformin Hydrochloride

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA076864

Marketing category

ANDA

Marketing start

2005-04-13

Marketing end

2020-06-30

Substance

METFORMIN HYDROCHLORIDE

Active strength

750 mg/1

Pharmacologic classes

Biguanide [EPC],Biguanides [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record