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Cefuroxime Axetil

NDC 16714-401 · NorthStar Rx LLC

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

Packages

16714-401-01 — 20 TABLET in 1 BOTTLE (16714-401-01)

16714-401-02 — 60 TABLET in 1 BOTTLE (16714-401-02)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0904-7542 — Cefuroxime axetil, 16714-400 — Cefuroxime Axetil, 43063-623 — Cefuroxime Axetil, 43063-656 — Cefuroxime axetil, 43063-657 — Cefuroxime axetil, 50090-0781 — Cefuroxime Axetil, 50090-0782 — Cefuroxime Axetil, 50090-2157 — Cefuroxime axetil, 50090-2158 — Cefuroxime axetil, 50090-2159 — Cefuroxime axetil, 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, +19 more

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