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CEFPODOXIME PROXETIL

NDC 65862-096 · Aurobindo Pharma Limited

Generic nameCEFPODOXIME PROXETIL
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)CEFPODOXIME PROXETIL
Strength200 mg/1
Pharmacologic classCephalosporin Antibacterial [EPC], Cephalosporins [CS]
Marketing categoryANDA

Packages

65862-096-01 — 100 TABLET, FILM COATED in 1 BOTTLE (65862-096-01)

65862-096-20 — 20 TABLET, FILM COATED in 1 BOTTLE (65862-096-20)

65862-096-25 — 250 TABLET, FILM COATED in 1 BOTTLE (65862-096-25)

65862-096-99 — 1000 TABLET, FILM COATED in 1 BOTTLE (65862-096-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0781-5439 — Cefpodoxime Proxetil, 16714-394 — CEFPODOXIME PROXETIL, 16714-395 — CEFPODOXIME PROXETIL, 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, 65862-140 — Cefpodoxime Proxetil, 65862-141 — Cefpodoxime Proxetil, 67877-559 — Cefpodoxime Proxetil, 67877-560 — Cefpodoxime Proxetil, 67877-878 — Cefpodoxime Proxetil, 67877-879 — Cefpodoxime Proxetil, 68071-3441 — Cefpodoxime Proxetil, 68071-3616 — Cefpodoxime Proxetil, 69043-006 — CEFPODOXIME PROXETIL, 69043-007 — 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.