Metronidazole

Product NDC

68788-7381

11-digit product format

687887381

Labeler code

68788

Product ID

68788-7381_a4a790a1-22a3-4b32-bd55-4c80f20b981e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metronidazole

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA070044

Marketing category

ANDA

Marketing start

2014-11-24

Marketing end

0000-00-00

Substance

METRONIDAZOLE

Active strength

500 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