Skip to main content

Cefpodoxime Proxetil

NDC 67877-878 · Ascend Laboratories, LLC

Generic nameCefpodoxime Proxetil
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)CEFPODOXIME PROXETIL
Strength100 mg/1
Pharmacologic classCephalosporin Antibacterial [EPC], Cephalosporins [CS]
Marketing categoryANDA

Packages

67877-878-01 — 100 TABLET, FILM COATED in 1 BOTTLE (67877-878-01)

67877-878-05 — 500 TABLET, FILM COATED in 1 BOTTLE (67877-878-05)

67877-878-20 — 20 TABLET, FILM COATED in 1 BOTTLE (67877-878-20)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

16714-402 — Cefpodoxime Proxetil, 16714-403 — Cefpodoxime Proxetil, 51407-083 — Cefpodoxime Proxetil, 51407-084 — Cefpodoxime Proxetil, 64980-402 — Cefpodoxime Proxetil, 64980-403 — Cefpodoxime Proxetil, 65862-095 — CEFPODOXIME PROXETIL, 65862-096 — CEFPODOXIME PROXETIL, 65862-140 — Cefpodoxime Proxetil, 65862-141 — Cefpodoxime Proxetil, 67877-559 — Cefpodoxime Proxetil, 67877-560 — Cefpodoxime Proxetil, 67877-879 — Cefpodoxime Proxetil, 68071-3441 — Cefpodoxime Proxetil, 68071-3616 — Cefpodoxime Proxetil, 69043-006 — CEFPODOXIME PROXETIL, 69043-007 — CEFPODOXIME PROXETIL, 69292-514 — Cefpodoxime Proxetil, 69292-516 — Cefpodoxime Proxetil, 70518-4676 — Cefpodoxime Proxetil, +4 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.