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"63323-341-29" National Drug Code (NDC)
Cefoxitin 25 VIAL in 1 CARTON (63323-341-29) / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-341-41)
(Fresenius Kabi USA, LLC)
NDC Code
63323-341-29
Package Description
25 VIAL in 1 CARTON (63323-341-29) / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-341-41)
Product NDC
63323-341
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Cefoxitin
Non-Proprietary Name
Cefoxitin Sodium
Dosage Form
POWDER, FOR SOLUTION
Usage
INTRAVENOUS
Start Marketing Date
20110706
Marketing Category Name
ANDA
Application Number
ANDA065414
Manufacturer
Fresenius Kabi USA, LLC
Substance Name
CEFOXITIN SODIUM
Strength
1
Strength Unit
g/1
Pharmacy Classes
Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/63323-341-29