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Cefuroxime axetil

NDC 60687-283 · American Health Packaging

Generic nameCefuroxime axetil
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)CEFUROXIME AXETIL
Strength500 mg/1
Pharmacologic classCephalosporin Antibacterial [EPC], Cephalosporins [CS]
Marketing categoryANDA

Packages

60687-283-94 — 20 BLISTER PACK in 1 CARTON (60687-283-94) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-283-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-4153 — Cefuroxime Axetil, 50090-6999 — Cefuroxime Axetil, 50090-7095 — Cefuroxime Axetil, 50090-7667 — Cefuroxime Axetil, 50090-7668 — Cefuroxime Axetil, 51407-333 — Cefuroxime axetil, 51407-334 — Cefuroxime axetil, 57237-058 — Cefuroxime Axetil, 57237-059 — Cefuroxime Axetil, 60687-272 — Cefuroxime axetil, 63187-991 — Cefuroxime axetil, 65862-698 — Cefuroxime Axetil, 65862-699 — Cefuroxime Axetil, 65862-700 — Cefuroxime Axetil, 67046-1081 — Cefuroxime Axetil, 67046-1307 — Cefuroxime Axetil, 67296-2168 — Cefuroxime axetil, 67296-2265 — Cefuroxime Axetil, 67877-215 — Cefuroxime axetil, 67877-216 — Cefuroxime axetil, +19 more

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