HALIBUT is a Percutaneous Injection, Solution in the Non-standardized Allergenic category. It is labeled and distributed by Alk-abello, Inc.. The primary component is Atlantic Halibut.
Product ID | 0268-7130_bc003fad-4700-4510-ab3f-3b284c703066 |
NDC | 0268-7130 |
Product Type | Non-standardized Allergenic |
Proprietary Name | HALIBUT |
Generic Name | Hippoglossus Hippoglossus |
Dosage Form | Injection, Solution |
Route of Administration | PERCUTANEOUS |
Marketing Start Date | 1965-01-01 |
Marketing Category | BLA / BLA |
Application Number | BLA103753 |
Labeler Name | ALK-Abello, Inc. |
Substance Name | ATLANTIC HALIBUT |
Active Ingredient Strength | 0 g/mL |
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 | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 1965-01-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | BLA |
Application Number | BLA103753 |
Product Type | NON-STANDARDIZED ALLERGENIC |
Marketing Start Date | 1965-01-01 |
Ingredient | Strength |
---|---|
ATLANTIC HALIBUT | .01 g/mL |
NDC | Brand Name | Generic Name |
---|---|---|
0268-6236 | HALIBUT | ATLANTIC HALIBUT |
0268-7130 | HALIBUT | HIPPOGLOSSUS HIPPOGLOSSUS |
36987-1218 | Halibut | Halibut |
36987-1219 | Halibut | Halibut |
36987-1220 | Halibut | Halibut |
36987-1221 | Halibut | Halibut |
49288-0251 | Halibut | Halibut |
49288-0252 | Halibut | Halibut |
54575-401 | HALIBUT | pacific halibut |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HALIBUT 88861382 not registered Live/Pending |
Koch OÃ 2020-04-06 |
HALIBUT 78686563 not registered Dead/Abandoned |
Laboratorios Andromaco Lda 2005-08-05 |