NDC 54575-346
PINTO BEAN
Kidney Bean
PINTO BEAN 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 Kidney Bean.
| Product ID | 54575-346_dbe7bebd-e445-4e59-8302-e706b795fbde |
| NDC | 54575-346 |
| Product Type | Human Prescription Drug |
| Proprietary Name | PINTO BEAN |
| Generic Name | Kidney Bean |
| 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 | KIDNEY BEAN |
| Active Ingredient Strength | 1 g/20mL |
| 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 | 2018-12-31 |
Packaging
NDC 54575-346-02
2 mL in 1 VIAL, MULTI-DOSE (54575-346-02)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 54575-346-02 [54575034602]
PINTO BEAN 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 54575-346-10 [54575034610]
PINTO BEAN 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 54575-346-30 [54575034630]
PINTO BEAN 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 54575-346-50 [54575034650]
PINTO BEAN 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 |
|---|---|
| KIDNEY BEAN | 1 g/20mL |
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 "Kidney Bean"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 49288-0046 | Pinto Bean | Pinto Bean |
| 54575-346 | PINTO BEAN | kidney bean |
| 0268-6107 | KIDNEY BEAN | KIDNEY BEAN |
| 49288-0061 | Kidney Bean | Kidney Bean |
| 54575-345 | NAVY BEAN | kidney bean |
| 54575-347 | RED KIDNEY 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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