Cefprozil

Product NDC

67253-232

11-digit product format

672530232

Labeler code

67253

Product ID

67253-232_f955de50-1f07-4079-9c2c-bd23ef54fd70

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefprozil

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

DAVA Pharmaceuticals Inc

Application

ANDA065235

Marketing category

ANDA

Marketing start

2014-08-01

Marketing end

2020-10-31

Substance

CEFPROZIL

Active strength

500 mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record