NDC 36987-1617
Chick Pea
Chick Pea
Chick Pea is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Nelco Laboratories, Inc.. The primary component is Chickpea.
| Product ID | 36987-1617_255e0c54-6613-460b-a91f-452fdfd0319d |
| NDC | 36987-1617 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Chick Pea |
| Generic Name | Chick Pea |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRADERMAL; SUBCUTANEOUS |
| Marketing Start Date | 1972-08-29 |
| Marketing Category | BLA / BLA |
| Application Number | BLA102192 |
| Labeler Name | Nelco Laboratories, Inc. |
| Substance Name | CHICKPEA |
| 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 36987-1617-2
10 mL in 1 VIAL, MULTI-DOSE (36987-1617-2)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 36987-1617-2 [36987161702]
Chick Pea INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
NDC 36987-1617-3 [36987161703]
Chick Pea INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
NDC 36987-1617-1 [36987161701]
Chick Pea INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
NDC 36987-1617-4 [36987161704]
Chick Pea INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| CHICKPEA | .1 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 "Chick Pea" or generic name "Chick Pea"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 36987-1614 | Chick Pea | Chick Pea |
| 36987-1615 | Chick Pea | Chick Pea |
| 36987-1616 | Chick Pea | Chick Pea |
| 36987-1617 | Chick Pea | Chick Pea |
Trademark Results [Chick Pea]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CHICK PEA 85663246 4316158 Live/Registered |
Cutie Pie Baby, Inc. 2012-06-27 |
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