NDC 54575-458
SHRIMP
Shrimp
SHRIMP 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 Shrimp.
| Product ID | 54575-458_dbe7bebd-e445-4e59-8302-e706b795fbde |
| NDC | 54575-458 |
| Product Type | Human Prescription Drug |
| Proprietary Name | SHRIMP |
| Generic Name | Shrimp |
| 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 | SHRIMP |
| 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],Shellfish Proteins [EXT] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
Packaging
NDC 54575-458-10
10 mL in 1 VIAL, MULTI-DOSE (54575-458-10)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 54575-458-30 [54575045830]
SHRIMP 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 54575-458-02 [54575045802]
SHRIMP 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 54575-458-50 [54575045850]
SHRIMP 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 54575-458-10 [54575045810]
SHRIMP 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 |
|---|---|
| SHRIMP | 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]
- Shellfish Proteins [EXT]
NDC Crossover Matching brand name "SHRIMP" or generic name "Shrimp"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0268-6214 | SHRIMP | COMMON SHRIMP |
| 22840-5778 | Shrimp | Farfantepenaeus aztecus |
| 36987-1258 | Shrimp | Shrimp |
| 36987-1259 | Shrimp | Shrimp |
| 36987-1260 | Shrimp | Shrimp |
| 36987-1261 | Shrimp | Shrimp |
| 49288-0478 | Shrimp | Shrimp |
| 54575-458 | SHRIMP | shrimp |
Trademark Results [SHRIMP]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SHRIMP 90547537 not registered Live/Pending |
KLX ENERGY SERVICES LLC 2021-02-25 |
 SHRIMP 77138243 3297158 Live/Registered |
Manley Laboratories Incorporated 2007-03-22 |
 SHRIMP 75434943 not registered Dead/Abandoned |
ReSound Corporation 1998-02-17 |
 SHRIMP 73585989 1416152 Dead/Cancelled |
QUAKER OATS COMPANY, THE 1986-03-03 |
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