Metronidazole

Product NDC

42292-001

11-digit product format

422920001

Labeler code

42292

Product ID

42292-001_7d002b16-cae7-5cee-e053-2991aa0ab577

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metronidazole

Dosage form

TABLET

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA070044

Marketing category

ANDA

Marketing start

2015-01-15

Marketing end

0000-00-00

Substance

METRONIDAZOLE

Active strength

500 mg/1

Pharmacologic classes

Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record