Metformin Hydrochloride

Product NDC

70518-0672

11-digit product format

705180672

Labeler code

70518

Product ID

70518-0672_7fafdef6-3904-823a-e053-2991aa0a7fb4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metformin Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA091184

Marketing category

ANDA

Marketing start

2017-08-16

Marketing end

0000-00-00

Substance

METFORMIN HYDROCHLORIDE

Active strength

1000 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