CODFISH 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 Cod.
Product ID | 54575-379_dbe7bebd-e445-4e59-8302-e706b795fbde |
NDC | 54575-379 |
Product Type | Human Prescription Drug |
Proprietary Name | CODFISH |
Generic Name | Cod |
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 | COD |
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],Fish Proteins, Dietary [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 |
---|---|
COD | 1 g/20mL |
NDC | Brand Name | Generic Name |
---|---|---|
0268-6128 | CODFISH | ATLANTIC COD |
36987-1202 | Codfish | Codfish |
36987-1203 | Codfish | Codfish |
36987-1204 | Codfish | Codfish |
36987-1205 | Codfish | Codfish |
54575-379 | CODFISH | cod |
49288-0147 | Cod | Cod |