NDC 54575-456
SCALLOP
Scallop
SCALLOP 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 Scallop.
| Product ID | 54575-456_dbe7bebd-e445-4e59-8302-e706b795fbde |
| NDC | 54575-456 |
| Product Type | Human Prescription Drug |
| Proprietary Name | SCALLOP |
| Generic Name | Scallop |
| 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 | SCALLOP |
| 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 54575-456-30
30 mL in 1 VIAL, MULTI-DOSE (54575-456-30)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 54575-456-30 [54575045630]
SCALLOP 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 54575-456-10 [54575045610]
SCALLOP 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 54575-456-02 [54575045602]
SCALLOP 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 54575-456-50 [54575045650]
SCALLOP 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 |
|---|---|
| SCALLOP | 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 "SCALLOP" or generic name "Scallop"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 36987-1254 | Scallop | Scallop |
| 36987-1255 | Scallop | Scallop |
| 36987-1256 | Scallop | Scallop |
| 36987-1257 | Scallop | Scallop |
| 54575-456 | SCALLOP | scallop |
Trademark Results [SCALLOP]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SCALLOP 97869899 not registered Live/Pending |
Xiamen Fengke E-commerce Co., Ltd. 2023-04-03 |
 SCALLOP 79199354 5343295 Live/Registered |
R82 A/S 2016-07-13 |
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