Metformin Hydrochloride

Product NDC

70518-0435

11-digit product format

705180435

Labeler code

70518

Product ID

70518-0435_850102f0-0296-2de8-e053-2a91aa0ad49c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metformin Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA075967

Marketing category

ANDA

Marketing start

2017-04-18

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