metronidazole

Product NDC

51672-5295

11-digit product format

516725295

Labeler code

51672

Product ID

51672-5295_f3698d33-814b-4ad1-8aa8-0728b8041dcc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

metronidazole

Dosage form

GEL

Route

TOPICAL

Labeler

Taro Pharmaceuticals U.S.A., Inc.

Application

NDA021789

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2005-06-30

Marketing end

0000-00-00

Substance

METRONIDAZOLE

Active strength

10 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