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Foscarnet Sodium - 0409-3863-05 - (Foscarnet Sodium)

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Drug Information of Foscarnet Sodium

Product NDC: 0409-3863
Proprietary Name: Foscarnet Sodium
Non Proprietary Name: Foscarnet Sodium
Active Ingredient(s): 24    mg/mL & nbsp;   Foscarnet Sodium
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Foscarnet Sodium

Product NDC: 0409-3863
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077174
Marketing Category: ANDA
Start Marketing Date: 20100707

Package Information of Foscarnet Sodium

Package NDC: 0409-3863-05
Package Description: 12 BOTTLE, GLASS in 1 CASE (0409-3863-05) > 500 mL in 1 BOTTLE, GLASS

NDC Information of Foscarnet Sodium

NDC Code 0409-3863-05
Proprietary Name Foscarnet Sodium
Package Description 12 BOTTLE, GLASS in 1 CASE (0409-3863-05) > 500 mL in 1 BOTTLE, GLASS
Product NDC 0409-3863
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Foscarnet Sodium
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20100707
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name FOSCARNET SODIUM
Strength Number 24
Strength Unit mg/mL
Pharmaceutical Classes DNA Polymerase Inhibitors [MoA],Pyrophosphate Analog [Chemical/Ingredient],Pyrophosphate Analog DNA Polymerase Inhibitor [EPC]

Complete Information of Foscarnet Sodium


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