Metronidazole

Product NDC

68788-9083

11-digit product format

687889083

Labeler code

68788

Product ID

68788-9083_2412148b-ccde-4c5d-8e7f-b5c4488d8f5a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metronidazole

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA070033

Marketing category

ANDA

Marketing start

2010-09-01

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

2019-12-31

Current FDA listing

Historical FDA.report record