NAFCILLIN - 0338-1019-48 - (NAFCILLIN)

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Drug Information of NAFCILLIN

Product NDC: 0338-1019
Proprietary Name: NAFCILLIN
Non Proprietary Name: NAFCILLIN
Active Ingredient(s): 2    g/100mL & nbsp;   NAFCILLIN
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of NAFCILLIN

Product NDC: 0338-1019
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050655
Marketing Category: NDA
Start Marketing Date: 19891031

Package Information of NAFCILLIN

Package NDC: 0338-1019-48
Package Description: 100 mL in 1 BAG (0338-1019-48)

NDC Information of NAFCILLIN

NDC Code 0338-1019-48
Proprietary Name NAFCILLIN
Package Description 100 mL in 1 BAG (0338-1019-48)
Product NDC 0338-1019
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NAFCILLIN
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19891031
Marketing Category Name NDA
Labeler Name Baxter Healthcare Corporation
Substance Name NAFCILLIN SODIUM
Strength Number 2
Strength Unit g/100mL
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of NAFCILLIN


General Information