Cefpodoxime Proxetil

Product NDC

0781-6169

11-digit product format

007816169

Labeler code

0781

Product ID

0781-6169_ca8fa9a5-094c-4c7e-8330-101ed5d68f6a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefpodoxime Proxetil

Dosage form

GRANULE, FOR SUSPENSION

Route

ORAL

Labeler

Sandoz Inc

Application

ANDA090031

Marketing category

ANDA

Marketing start

2009-06-25

Marketing end

2019-07-31

Substance

CEFPODOXIME PROXETIL

Active strength

100 mg/5mL

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record