NDC 54575-342
BLACK BASS
Largemouth Bass
BLACK BASS 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 Largemouth Bass.
| Product ID | 54575-342_dbe7bebd-e445-4e59-8302-e706b795fbde |
| NDC | 54575-342 |
| Product Type | Human Prescription Drug |
| Proprietary Name | BLACK BASS |
| Generic Name | Largemouth Bass |
| 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 | LARGEMOUTH BASS |
| 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 |
Packaging
NDC 54575-342-50
50 mL in 1 VIAL, MULTI-DOSE (54575-342-50)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 54575-342-50 [54575034250]
BLACK BASS INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2020-01-31 |
NDC 54575-342-30 [54575034230]
BLACK BASS INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2020-01-31 |
NDC 54575-342-02 [54575034202]
BLACK BASS INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2020-01-31 |
NDC 54575-342-10 [54575034210]
BLACK BASS INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2020-01-31 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| LARGEMOUTH BASS | 1 g/20mL |
OpenFDA Data
Pharmacological Class
- Non-Standardized Food Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Allergens [CS]
- Dietary Proteins [CS]
- Fish Proteins
- Dietary [EXT]
NDC Crossover Matching brand name "BLACK BASS" or generic name "Largemouth Bass"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 22840-5766 | Black Bass | Centropristis striata |
| 54575-342 | BLACK BASS | largemouth bass |
Trademark Results [BLACK BASS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BLACK BASS 87980635 5761070 Live/Registered |
BISON UNION IP HOLDINGS LLC 2018-06-12 |
 BLACK BASS 87958862 not registered Dead/Abandoned |
BISON UNION IP HOLDINGS LLC 2018-06-12 |
 BLACK BASS 74002104 1680465 Dead/Cancelled |
HOT-B USA INC. 1989-11-16 |
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