NDC 49288-0384
Black Pepper
Black Pepper
Black Pepper 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 Pepper.
| Product ID | 49288-0384_1d11d7ba-8b48-401c-a02e-42b54abb4296 |
| NDC | 49288-0384 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Black Pepper |
| Generic Name | Black Pepper |
| 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 PEPPER |
| 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],Vegetable Proteins [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 49288-0384-1
2 mL in 1 VIAL, MULTI-DOSE (49288-0384-1)
| Marketing Start Date | 1974-03-23 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 49288-0384-1 [49288038401]
Black Pepper 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 49288-0384-2 [49288038402]
Black Pepper 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 49288-0384-3 [49288038403]
Black Pepper 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 49288-0384-5 [49288038405]
Black Pepper 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 49288-0384-4 [49288038404]
Black Pepper 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 PEPPER | .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]
- Vegetable Proteins [CS]
NDC Crossover Matching brand name "Black Pepper" or generic name "Black Pepper"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0268-6198 | BLACK PEPPER | BLACK PEPPER |
| 22840-5740 | Black Pepper | Piper nigrum |
| 36987-1766 | Black Pepper | Black Pepper |
| 36987-1767 | Black Pepper | Black Pepper |
| 36987-1768 | Black Pepper | Black Pepper |
| 36987-1769 | Black Pepper | Black Pepper |
| 49288-0384 | Black Pepper | Black Pepper |
| 54575-436 | BLACK PEPPER | black pepper |
Trademark Results [Black Pepper]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BLACK PEPPER 79206370 5430456 Live/Registered |
Monsieur DOUMITH David 2017-02-14 |
 BLACK PEPPER 79001126 3129963 Dead/Cancelled |
Monsieur DOUMITH David 2004-01-20 |
 BLACK PEPPER 75218330 2208023 Dead/Cancelled |
Doumith, David 1996-12-24 |
 BLACK PEPPER 73320602 not registered Dead/Abandoned |
BREAKAWAY SPORTSWEAR PTY. LTD. 0000-00-00 |
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