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Albuminar-20 - 0053-7695-33 - (Albumin Human)

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Drug Information of Albuminar-20

Product NDC: 0053-7695
Proprietary Name: Albuminar-20
Non Proprietary Name: Albumin Human
Active Ingredient(s): 20    g/100mL & nbsp;   Albumin Human
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Albuminar-20

Product NDC: 0053-7695
Labeler Name: CSL Behring LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA103955
Marketing Category: BLA
Start Marketing Date: 20090106

Package Information of Albuminar-20

Package NDC: 0053-7695-33
Package Description: 1 VIAL, GLASS in 1 CARTON (0053-7695-33) > 50 mL in 1 VIAL, GLASS

NDC Information of Albuminar-20

NDC Code 0053-7695-33
Proprietary Name Albuminar-20
Package Description 1 VIAL, GLASS in 1 CARTON (0053-7695-33) > 50 mL in 1 VIAL, GLASS
Product NDC 0053-7695
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Albumin Human
Dosage Form Name SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20090106
Marketing Category Name BLA
Labeler Name CSL Behring LLC
Substance Name ALBUMIN HUMAN
Strength Number 20
Strength Unit g/100mL
Pharmaceutical Classes Human Serum Albumin [EPC],Increased Intravascular Volume [PE],Increased Oncotic Pressure [PE],Osmotic Activity [MoA],Serum Albumin [Chemical/Ingredient]

Complete Information of Albuminar-20


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