Product NDC: | 54575-333 |
Proprietary Name: | ALMOND |
Non Proprietary Name: | almond |
Active Ingredient(s): | 1 g/20mL & nbsp; almond |
Administration Route(s): | PERCUTANEOUS; SUBCUTANEOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54575-333 |
Labeler Name: | Allergy Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA101376 |
Marketing Category: | BLA |
Start Marketing Date: | 19671207 |
Package NDC: | 54575-333-50 |
Package Description: | 50 mL in 1 VIAL, MULTI-DOSE (54575-333-50) |
NDC Code | 54575-333-50 |
Proprietary Name | ALMOND |
Package Description | 50 mL in 1 VIAL, MULTI-DOSE (54575-333-50) |
Product NDC | 54575-333 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | almond |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | PERCUTANEOUS; SUBCUTANEOUS |
Start Marketing Date | 19671207 |
Marketing Category Name | BLA |
Labeler Name | Allergy Laboratories, Inc. |
Substance Name | ALMOND |
Strength Number | 1 |
Strength Unit | g/20mL |
Pharmaceutical Classes | Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Nut Proteins [Chemical/Ingredient] |