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Nafcillin Sodium - 0781-3128-92 - (Nafcillin Sodium)

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Drug Information of Nafcillin Sodium

Product NDC: 0781-3128
Proprietary Name: Nafcillin Sodium
Non Proprietary Name: Nafcillin Sodium
Active Ingredient(s): 1    g/1 & nbsp;   Nafcillin Sodium
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Nafcillin Sodium

Product NDC: 0781-3128
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062732
Marketing Category: ANDA
Start Marketing Date: 20050923

Package Information of Nafcillin Sodium

Package NDC: 0781-3128-92
Package Description: 10 VIAL, PATENT DELIVERY SYSTEM in 1 PACKAGE (0781-3128-92) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PATENT DELIVERY SYSTEM (0781-3128-15)

NDC Information of Nafcillin Sodium

NDC Code 0781-3128-92
Proprietary Name Nafcillin Sodium
Package Description 10 VIAL, PATENT DELIVERY SYSTEM in 1 PACKAGE (0781-3128-92) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PATENT DELIVERY SYSTEM (0781-3128-15)
Product NDC 0781-3128
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nafcillin Sodium
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20050923
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name NAFCILLIN SODIUM
Strength Number 1
Strength Unit g/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

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