Cefuroxime Axetil

Product NDC

68788-9914

11-digit product format

687889914

Labeler code

68788

Product ID

68788-9914_7e2495ea-48fe-4f4f-9531-f42fa043a69b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefuroxime Axetil

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticali Inc.

Application

ANDA065308

Marketing category

ANDA

Marketing start

2015-05-19

Marketing end

0000-00-00

Substance

CEFUROXIME AXETIL

Active strength

500 mg/1

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record