Cefoxitin

NDC 63323-342 · Fresenius Kabi USA, LLC

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

Generic nameCefoxitin Sodium

Dosage formPOWDER, FOR SOLUTION

RouteINTRAVENOUS

Active ingredient(s)CEFOXITIN SODIUM

Strength2 g/1

Pharmacologic classCephalosporin Antibacterial [EPC], Cephalosporins [CS]

Marketing categoryANDA

Packages

63323-342-29 — 25 VIAL in 1 CARTON (63323-342-29) / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-342-41)

63323-342-25 — 25 VIAL in 1 CARTON (63323-342-25) / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-342-01)

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, 44567-245 — Cefoxitin, 44567-246 — Cefoxitin, 44567-247 — Cefoxitin, 63323-341 — 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.