Metronidazole Topical Gel

Product NDC

69007-835

11-digit product format

690070835

Labeler code

69007

Product ID

69007-835_960347a4-11bd-4c23-84a8-d4a3d9eafe1d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

metronidazole

Dosage form

GEL

Route

TOPICAL

Labeler

Owen Laboratories

Application

NDA019737

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2014-03-01

Marketing end

0000-00-00

Substance

METRONIDAZOLE

Active strength

8 mg/g

Pharmacologic classes

Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record