Product NDC: | 49288-0046 |
Proprietary Name: | Pinto Bean |
Non Proprietary Name: | Pinto Bean |
Active Ingredient(s): | .05 g/mL & nbsp; Pinto Bean |
Administration Route(s): | INTRADERMAL; SUBCUTANEOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49288-0046 |
Labeler Name: | Antigen Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA102223 |
Marketing Category: | BLA |
Start Marketing Date: | 19740323 |
Package NDC: | 49288-0046-3 |
Package Description: | 10 mL in 1 VIAL, MULTI-DOSE (49288-0046-3) |
NDC Code | 49288-0046-3 |
Proprietary Name | Pinto Bean |
Package Description | 10 mL in 1 VIAL, MULTI-DOSE (49288-0046-3) |
Product NDC | 49288-0046 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Pinto Bean |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRADERMAL; SUBCUTANEOUS |
Start Marketing Date | 19740323 |
Marketing Category Name | BLA |
Labeler Name | Antigen Laboratories, Inc. |
Substance Name | KIDNEY BEAN |
Strength Number | .05 |
Strength Unit | g/mL |
Pharmaceutical Classes | Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient],Vegetable Proteins [Chemical/Ingredient] |