Metronidazole

Product NDC

50268-539

11-digit product format

502680539

Labeler code

50268

Product ID

50268-539_7e7c3128-d1ae-8a4a-e053-2991aa0a770e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metronidazole

Dosage form

TABLET

Route

ORAL

Labeler

AvPAK

Application

ANDA070044

Marketing category

ANDA

Marketing start

2016-11-08

Marketing end

2019-03-31

Substance

METRONIDAZOLE

Active strength

500 mg/1

Pharmacologic classes

Nitroimidazole

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record