Product NDC: | 49288-0592 |
Proprietary Name: | Venison |
Non Proprietary Name: | Venison |
Active Ingredient(s): | .05 g/mL & nbsp; Venison |
Administration Route(s): | INTRADERMAL; SUBCUTANEOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49288-0592 |
Labeler Name: | Antigen Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA102223 |
Marketing Category: | BLA |
Start Marketing Date: | 19740323 |
Package NDC: | 49288-0592-5 |
Package Description: | 50 mL in 1 VIAL, MULTI-DOSE (49288-0592-5) |
NDC Code | 49288-0592-5 |
Proprietary Name | Venison |
Package Description | 50 mL in 1 VIAL, MULTI-DOSE (49288-0592-5) |
Product NDC | 49288-0592 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Venison |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRADERMAL; SUBCUTANEOUS |
Start Marketing Date | 19740323 |
Marketing Category Name | BLA |
Labeler Name | Antigen Laboratories, Inc. |
Substance Name | VENISON |
Strength Number | .05 |
Strength Unit | g/mL |
Pharmaceutical Classes | Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Meat Proteins [Chemical/Ingredient] |