NDC 0143-9878 – Cefoxitin

Cefoxitin Sodium 1 g/1 · Injection, Powder, For Solution · Intravenous

Human Prescription Drug

Product NDC0143-9878

Product details

Brand name
Cefoxitin
Generic name
Cefoxitin
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Injection, Powder, For Solution
Route
Intravenous
Marketing category
ANDA · ANDA065238
Marketed since
March 12, 2010
Listing expires
December 31, 2026
Pharmacologic class
Cephalosporin Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Cefoxitin →

Package NDC codes (1)

Package NDCDescriptionSince
0143-9878-2525 VIAL in 1 CARTON (0143-9878-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9878-01)Mar 12, 2010

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