NDC 49288-0595
Whole Wheat
Whole Wheat
Whole Wheat 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 Wheat.
| Product ID | 49288-0595_1d11d7ba-8b48-401c-a02e-42b54abb4296 |
| NDC | 49288-0595 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Whole Wheat |
| Generic Name | Whole Wheat |
| 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 | WHEAT |
| 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],Grain Proteins [EXT] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 49288-0595-1
2 mL in 1 VIAL, MULTI-DOSE (49288-0595-1)
| Marketing Start Date | 1974-03-23 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 49288-0595-2 [49288059502]
Whole Wheat 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 49288-0595-3 [49288059503]
Whole Wheat 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 49288-0595-5 [49288059505]
Whole Wheat 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 49288-0595-4 [49288059504]
Whole Wheat 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 49288-0595-1 [49288059501]
Whole Wheat 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 |
|---|---|
| WHEAT | .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]
- Grain Proteins [EXT]
NDC Crossover Matching brand name "Whole Wheat" or generic name "Whole Wheat"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 22840-5756 | Whole Wheat | Triticum aestivum |
| 49288-0595 | Whole Wheat | Whole Wheat |
Trademark Results [Whole Wheat]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 WHOLE WHEAT 88234507 not registered Dead/Abandoned |
SUN, PATRICIA MULIAWATI 2018-12-19 |
 WHOLE WHEAT 76700466 4016159 Dead/Cancelled |
Oshry, Scott 2009-11-20 |
 WHOLE WHEAT 75602940 not registered Dead/Abandoned |
GRISMER, TOM A. 1998-12-10 |
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