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GAMMAGARD LIQUID - 0944-2700-05 - (Human Immunoglobulin G)

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Drug Information of GAMMAGARD LIQUID

Product NDC: 0944-2700
Proprietary Name: GAMMAGARD LIQUID
Non Proprietary Name: Human Immunoglobulin G
Active Ingredient(s): 100    mg/mL & nbsp;   Human Immunoglobulin G
Administration Route(s): INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of GAMMAGARD LIQUID

Product NDC: 0944-2700
Labeler Name: Baxter Healthcare Corporation
Product Type: PLASMA DERIVATIVE
FDA Application Number: BLA125105
Marketing Category: BLA
Start Marketing Date: 20050427

Package Information of GAMMAGARD LIQUID

Package NDC: 0944-2700-05
Package Description: 1 BOTTLE, GLASS in 1 CARTON (0944-2700-05) > 100 mL in 1 BOTTLE, GLASS

NDC Information of GAMMAGARD LIQUID

NDC Code 0944-2700-05
Proprietary Name GAMMAGARD LIQUID
Package Description 1 BOTTLE, GLASS in 1 CARTON (0944-2700-05) > 100 mL in 1 BOTTLE, GLASS
Product NDC 0944-2700
Product Type Name PLASMA DERIVATIVE
Non Proprietary Name Human Immunoglobulin G
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20050427
Marketing Category Name BLA
Labeler Name Baxter Healthcare Corporation
Substance Name HUMAN IMMUNOGLOBULIN G
Strength Number 100
Strength Unit mg/mL
Pharmaceutical Classes Human Immunoglobulin G [EPC],Passively Acquired Immunity [PE],Antigen Neutralization [MoA],Immunoglobulins [Chemical/Ingredient]

Complete Information of GAMMAGARD LIQUID


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