CASHEW NUT is a Percutaneous; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Allergy Laboratories, Inc.. The primary component is Cashew.
Product ID | 54575-364_dbe7bebd-e445-4e59-8302-e706b795fbde |
NDC | 54575-364 |
Product Type | Human Prescription Drug |
Proprietary Name | CASHEW NUT |
Generic Name | Cashew |
Dosage Form | Injection, Solution |
Route of Administration | PERCUTANEOUS; SUBCUTANEOUS |
Marketing Start Date | 1972-08-29 |
Marketing Category | BLA / BLA |
Application Number | BLA102192 |
Labeler Name | Allergy Laboratories, Inc. |
Substance Name | CASHEW |
Active Ingredient Strength | 1 g/20mL |
Pharm Classes | Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Nut Proteins [EXT] |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 1972-08-29 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | BLA |
Application Number | BLA102192 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1972-08-29 |
Inactivation Date | 2020-01-31 |
Marketing Category | BLA |
Application Number | BLA102192 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1972-08-29 |
Inactivation Date | 2020-01-31 |
Marketing Category | BLA |
Application Number | BLA102192 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1972-08-29 |
Inactivation Date | 2020-01-31 |
Marketing Category | BLA |
Application Number | BLA102192 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1972-08-29 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
CASHEW | 1 g/20mL |
NDC | Brand Name | Generic Name |
---|---|---|
22840-5783 | Cashew Nut | Anacardium occidentale |
54575-364 | CASHEW NUT | cashew |
36987-1534 | Cashew | Cashew |
36987-1535 | Cashew | Cashew |
36987-1536 | Cashew | Cashew |
36987-1537 | Cashew | Cashew |