METRONIDAZOLE

Product NDC

69007-836

11-digit product format

690070836

Labeler code

69007

Product ID

69007-836_cd7304d0-0ac9-40d9-bc8b-8656d637f9fe

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

METRONIDAZOLE

Dosage form

CREAM

Route

TOPICAL

Labeler

Owen Laboratories

Application

NDA020531

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2009-06-18

Marketing end

0000-00-00

Substance

METRONIDAZOLE

Active strength

8 mg/g

Pharmacologic classes

Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record