Product NDC: | 13533-700 |
Proprietary Name: | PROLASTIN-C |
Non Proprietary Name: | alpha-1-proteinase inhibitor human |
Active Ingredient(s): | & nbsp; alpha-1-proteinase inhibitor human |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 13533-700 |
Labeler Name: | Grifols Therapeutics Inc. |
Product Type: | PLASMA DERIVATIVE |
FDA Application Number: | BLA103174 |
Marketing Category: | BLA |
Start Marketing Date: | 19871202 |
Package NDC: | 13533-700-01 |
Package Description: | 1 KIT in 1 CARTON (13533-700-01) * 20 mL in 1 VIAL, SINGLE-DOSE * 20 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 13533-700-01 |
Proprietary Name | PROLASTIN-C |
Package Description | 1 KIT in 1 CARTON (13533-700-01) * 20 mL in 1 VIAL, SINGLE-DOSE * 20 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 13533-700 |
Product Type Name | PLASMA DERIVATIVE |
Non Proprietary Name | alpha-1-proteinase inhibitor human |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 19871202 |
Marketing Category Name | BLA |
Labeler Name | Grifols Therapeutics Inc. |
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