Metronidazole

Product NDC

51655-123

11-digit product format

516550123

Labeler code

51655

Product ID

51655-123_4a3e2edf-4f5e-66a9-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metronidazole

Dosage form

TABLET

Route

ORAL

Labeler

Northwind Pharmaceuticals

Application

ANDA079067

Marketing category

ANDA

Marketing start

2014-12-16

Marketing end

0000-00-00

Substance

METRONIDAZOLE

Active strength

250 mg/1

Pharmacologic classes

Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record