Metronidazole

Product NDC

71335-0874

11-digit product format

713350874

Labeler code

71335

Product ID

71335-0874_0eef6419-0183-4ea6-b331-00c615915ecd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metronidazole

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA070035

Marketing category

ANDA

Marketing start

2011-11-17

Marketing end

0000-00-00

Substance

METRONIDAZOLE

Active strength

250 mg/1

Pharmacologic classes

Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record