Cefoxitin

NDC 44567-245 · WG Critical Care, LLC

FDA carries 2 listing records for this NDC; the most recent is shown.

Generic nameCefoxitin

Dosage formINJECTION, POWDER, FOR SOLUTION

RouteINTRAVENOUS

Active ingredient(s)CEFOXITIN SODIUM

Strength1 g/1

Pharmacologic classCephalosporin Antibacterial [EPC], Cephalosporins [CS]

Marketing categoryANDA

Packages

44567-245-85 — 25 VIAL in 1 CARTON (44567-245-85) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

44567-245-25 — 25 VIAL in 1 CARTON (44567-245-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

J0694 — Injection, cefoxitin sodium, 1 gm Medicare Part B payment limit (ASP + 6%): $4.29

FDA lists these products with the same active ingredient.

0143-9876 — Cefoxitin, 0143-9877 — Cefoxitin, 0143-9878 — Cefoxitin, 0264-3123 — CEFOXITIN SODIUM, 0264-3125 — CEFOXITIN SODIUM, 25021-109 — cefoxitin, 25021-110 — cefoxitin, 25021-111 — cefoxitin, 44567-246 — Cefoxitin, 44567-247 — Cefoxitin, 63323-341 — Cefoxitin Sodium, 63323-342 — Cefoxitin Sodium, 66288-4100 — cefoxitin

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.