NDC 49288-0381
Black-eyed Pea
Black-eyed Pea
Black-eyed Pea is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Antigen Laboratories, Inc.. The primary component is Black-eyed Pea.
| Product ID | 49288-0381_1d11d7ba-8b48-401c-a02e-42b54abb4296 |
| NDC | 49288-0381 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Black-eyed Pea |
| Generic Name | Black-eyed Pea |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRADERMAL; SUBCUTANEOUS |
| Marketing Start Date | 1974-03-23 |
| Marketing Category | BLA / BLA |
| Application Number | BLA102223 |
| Labeler Name | Antigen Laboratories, Inc. |
| Substance Name | BLACK-EYED PEA |
| 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] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 49288-0381-5
50 mL in 1 VIAL, MULTI-DOSE (49288-0381-5)
| Marketing Start Date | 1974-03-23 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 49288-0381-3 [49288038103]
Black-eyed Pea INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0381-5 [49288038105]
Black-eyed Pea INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0381-2 [49288038102]
Black-eyed Pea INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0381-1 [49288038101]
Black-eyed Pea INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0381-4 [49288038104]
Black-eyed Pea INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| BLACK-EYED PEA | .05 g/mL |
OpenFDA Data
Pharmacological Class
- Non-Standardized Food Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Allergens [CS]
- Dietary Proteins [CS]
NDC Crossover Matching brand name "Black-eyed Pea" or generic name "Black-eyed Pea"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 49288-0381 | Black-eyed Pea | Black-eyed Pea |
| 54575-430 | BLACKEYED PEA | black-eyed pea |
Trademark Results [Black-eyed Pea]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BLACK-EYED PEA 75392380 2427766 Live/Registered |
RMR COLORADO, LLC 1997-11-18 |
 BLACK-EYED PEA 73679377 1486543 Live/Registered |
PRUFROCK RESTAURANTS, INC. 1987-08-19 |
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