FDA NDC

Cefoxitin

This name is from the loaded FDA file.

Source: FDA NDC Directory, live from openFDA. Publisher page

NDC
63323-341
Proprietary name
Cefoxitin
Nonproprietary name
Cefoxitin Sodium
Labeler
Fresenius Kabi USA, LLC
Dosage form
POWDER, FOR SOLUTION
Strength
1 g/1

HCPCS J3373 Billable units per 11-digit NDC: 1000.

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