METFORMIN HYDROCHLORIDE

Product NDC

70934-311

11-digit product format

709340311

Labeler code

70934

Product ID

70934-311_8957a587-ec5e-adb7-e053-2995a90a26a9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

METFORMIN HYDROCHLORIDE

Dosage form

TABLET, COATED

Route

ORAL

Labeler

Denton Pharma, Inc. DBA Northwind Pharmaceuticals

Application

ANDA205096

Marketing category

ANDA

Marketing start

2019-03-11

Marketing end

0000-00-00

Substance

METFORMIN HYDROCHLORIDE

Active strength

500 mg/1

Pharmacologic classes

Biguanide [EPC],Biguanides [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record