NDC 0781-5439 – Cefpodoxime Proxetil

Cefpodoxime Proxetil 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC0781-5439

Product details

Brand name
Cefpodoxime Proxetil
Generic name
Cefpodoxime Proxetil
Labeler
Sandoz Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA065462
Marketed since
May 28, 2008
Listing expires
December 31, 2027
Pharmacologic class
Cephalosporin Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Cefpodoxime Proxetil →

Package NDC codes (2)

Package NDCDescriptionSince
0781-5439-01100 TABLET, FILM COATED in 1 BOTTLE (0781-5439-01)May 28, 2008
0781-5439-2020 TABLET, FILM COATED in 1 BOTTLE (0781-5439-20)May 28, 2008

Recalls mentioning this NDC

Other Cefpodoxime Proxetil products