Metronidazole

Product NDC

68788-8930

11-digit product format

687888930

Labeler code

68788

Product ID

68788-8930_e72cd7fd-f84d-4e77-baf6-190aaae75787

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metronidazole

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA070035

Marketing category

ANDA

Marketing start

2015-10-08

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