NDC 49288-0046
Pinto Bean
Pinto Bean
Pinto Bean 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 Kidney Bean.
| Product ID | 49288-0046_1d11d7ba-8b48-401c-a02e-42b54abb4296 |
| NDC | 49288-0046 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Pinto Bean |
| Generic Name | Pinto Bean |
| 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 | KIDNEY BEAN |
| Active Ingredient Strength | 0 g/mL |
| Pharm Classes | Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Vegetable Proteins [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 49288-0046-3
10 mL in 1 VIAL, MULTI-DOSE (49288-0046-3)
| Marketing Start Date | 1974-03-23 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 49288-0046-4 [49288004604]
Pinto Bean 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 49288-0046-3 [49288004603]
Pinto Bean 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 49288-0046-1 [49288004601]
Pinto Bean 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 49288-0046-2 [49288004602]
Pinto Bean 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 49288-0046-5 [49288004605]
Pinto Bean 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 |
|---|---|
| KIDNEY BEAN | .05 g/mL |
OpenFDA Data
Pharmacological Class
- Non-Standardized Plant Allergenic Extract [EPC]
- Non-Standardized Food Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Allergens [CS]
- Dietary Proteins [CS]
- Plant Proteins [CS]
- Vegetable Proteins [CS]
NDC Crossover Matching brand name "Pinto Bean" or generic name "Pinto Bean"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 49288-0046 | Pinto Bean | Pinto Bean |
| 54575-346 | PINTO BEAN | kidney bean |
Trademark Results [Pinto Bean]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PINTO BEAN 78334178 not registered Dead/Abandoned |
Pinto Bean, LLC 2003-11-29 |
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