Metronidazole

Product NDC

42708-064

11-digit product format

427080064

Labeler code

42708

Product ID

42708-064_da4ac6ee-ea53-45a7-8f37-71536a67aa79

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metronidazole

Dosage form

TABLET

Route

ORAL

Labeler

QPharma Inc

Application

ANDA070033

Marketing category

ANDA

Marketing start

1990-09-30

Marketing end

0000-00-00

Substance

METRONIDAZOLE

Active strength

500 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