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Human Albumin Grifols - 61953-0002-1 - (Albumin (Human))

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Drug Information of Human Albumin Grifols

Product NDC: 61953-0002
Proprietary Name: Human Albumin Grifols
Non Proprietary Name: Albumin (Human)
Active Ingredient(s): 12.5    g/50mL & nbsp;   Albumin (Human)
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Human Albumin Grifols

Product NDC: 61953-0002
Labeler Name: Instituto Grifols, S.A.
Product Type: PLASMA DERIVATIVE
FDA Application Number: BLA103352
Marketing Category: BLA
Start Marketing Date: 20030611

Package Information of Human Albumin Grifols

Package NDC: 61953-0002-1
Package Description: 1 VIAL in 1 CARTON (61953-0002-1) > 50 mL in 1 VIAL (61953-0002-3)

NDC Information of Human Albumin Grifols

NDC Code 61953-0002-1
Proprietary Name Human Albumin Grifols
Package Description 1 VIAL in 1 CARTON (61953-0002-1) > 50 mL in 1 VIAL (61953-0002-3)
Product NDC 61953-0002
Product Type Name PLASMA DERIVATIVE
Non Proprietary Name Albumin (Human)
Dosage Form Name SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20030611
Marketing Category Name BLA
Labeler Name Instituto Grifols, S.A.
Substance Name ALBUMIN (HUMAN)
Strength Number 12.5
Strength Unit g/50mL
Pharmaceutical Classes Human Serum Albumin [EPC],Increased Intravascular Volume [PE],Increased Oncotic Pressure [PE],Osmotic Activity [MoA],Serum Albumin [Chemical/Ingredient]

Complete Information of Human Albumin Grifols


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