NDC 63323-342 – Cefoxitin

Cefoxitin Sodium 2 g/1 · Powder, For Solution · Intravenous

Human Prescription Drug

Product NDC63323-342

Product details

Brand name
Cefoxitin
Generic name
Cefoxitin Sodium
Labeler
Fresenius Kabi USA, LLC
Dosage form
Powder, For Solution
Route
Intravenous
Marketing category
ANDA · ANDA065414
Marketed since
July 6, 2011
Listing expires
December 31, 2026
Pharmacologic class
Cephalosporin Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Cefoxitin →

Package NDC codes (2)

Package NDCDescriptionSince
63323-342-2525 VIAL in 1 CARTON (63323-342-25) / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-342-01)Jul 6, 2011
63323-342-2925 VIAL in 1 CARTON (63323-342-29) / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-342-41)Jul 6, 2011

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