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 |