cefuroxime axetil

Product NDC

50090-0798

11-digit product format

500900798

Labeler code

50090

Product ID

50090-0798_0e5553e2-87eb-4175-bc04-3b9a2d34e71f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

cefuroxime axetil

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA065135

Marketing category

ANDA

Marketing start

2003-07-25

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