Metformin Hydrochloride

Product NDC

50268-532

11-digit product format

502680532

Labeler code

50268

Product ID

50268-532_77f523e0-7ffc-94f8-e053-2991aa0a1c9b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metformin Hydrochloride

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

AvPAK

Application

ANDA078596

Marketing category

ANDA

Marketing start

2014-11-17

Marketing end

0000-00-00

Substance

METFORMIN HYDROCHLORIDE

Active strength

750 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