METRONIDAZOLE

Product NDC

60760-334

11-digit product format

607600334

Labeler code

60760

Product ID

60760-334_7abc876a-7c42-97e0-e053-2991aa0a84fd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

METRONIDAZOLE

Dosage form

TABLET

Route

ORAL

Labeler

St Marys Medical Park Pharmacy

Application

ANDA070033

Marketing category

ANDA

Marketing start

2013-01-10

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