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Cefuroxime Axetil

NDC 68071-3899 · NuCare Pharmaceuticals, Inc.

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

68071-3899-4 — 14 TABLET, FILM COATED in 1 BOTTLE (68071-3899-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

57237-059 — Cefuroxime Axetil, 60687-272 — Cefuroxime axetil, 60687-283 — 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, 68071-1637 — Cefuroxime axetil, 68071-3975 — Cefuroxime axetil, 68071-4947 — Cefuroxime axetil, 68788-8905 — Cefuroxime Axetil, 70518-3215 — Cefuroxime Axetil, 72789-035 — Cefuroxime axetil, 80425-0571 — 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.