Product NDC: | 54575-436 |
Proprietary Name: | BLACK PEPPER |
Non Proprietary Name: | black pepper |
Active Ingredient(s): | 1 g/20mL & nbsp; black pepper |
Administration Route(s): | PERCUTANEOUS; SUBCUTANEOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54575-436 |
Labeler Name: | Allergy Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA102192 |
Marketing Category: | BLA |
Start Marketing Date: | 19720829 |
Package NDC: | 54575-436-50 |
Package Description: | 50 mL in 1 VIAL, MULTI-DOSE (54575-436-50) |
NDC Code | 54575-436-50 |
Proprietary Name | BLACK PEPPER |
Package Description | 50 mL in 1 VIAL, MULTI-DOSE (54575-436-50) |
Product NDC | 54575-436 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | black pepper |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | PERCUTANEOUS; SUBCUTANEOUS |
Start Marketing Date | 19720829 |
Marketing Category Name | BLA |
Labeler Name | Allergy Laboratories, Inc. |
Substance Name | BLACK PEPPER |
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],Vegetable Proteins [Chemical/Ingredient] |