Metronidazole

Product NDC

51079-216

11-digit product format

510790216

Labeler code

51079

Product ID

51079-216_7d0036d9-0375-6900-e053-2991aa0a8aec

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metronidazole

Dosage form

TABLET

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA070035

Marketing category

ANDA

Marketing start

2012-08-20

Marketing end

2019-04-30

Substance

METRONIDAZOLE

Active strength

250 mg/1

Pharmacologic classes

Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record