Metronidazole

Product NDC

68788-9372

11-digit product format

687889372

Labeler code

68788

Product ID

68788-9372_48d2d9b7-05e2-44b5-b6a5-056eb28025ab

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metronidazole

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA079067

Marketing category

ANDA

Marketing start

2014-10-07

Marketing end

0000-00-00

Substance

METRONIDAZOLE

Active strength

250 mg/1

Pharmacologic classes

Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record