NDC 36987-1604
Leeks
Leeks
Leeks 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 Leek.
| Product ID | 36987-1604_20425e8b-8db3-4a2b-813b-7e3e1bc1c4e6 |
| NDC | 36987-1604 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Leeks |
| Generic Name | Leeks |
| 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 | LEEK |
| Active Ingredient Strength | 0 g/mL |
| Pharm Classes | Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Non-Standardized Food Allergenic Extract [EPC],Vegetable Proteins [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 36987-1604-3
30 mL in 1 VIAL, MULTI-DOSE (36987-1604-3)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 36987-1604-3 [36987160403]
Leeks 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 36987-1604-4 [36987160404]
Leeks 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 36987-1604-1 [36987160401]
Leeks 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 36987-1604-2 [36987160402]
Leeks 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 |
|---|---|
| LEEK | .1 g/mL |
OpenFDA Data
Pharmacological Class
- Non-Standardized Plant Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Allergens [CS]
- Dietary Proteins [CS]
- Plant Proteins [CS]
- Non-Standardized Food Allergenic Extract [EPC]
- Vegetable Proteins [CS]
NDC Crossover Matching brand name "Leeks" or generic name "Leeks"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 36987-1602 | Leeks | Leeks |
| 36987-1603 | Leeks | Leeks |
| 36987-1604 | Leeks | Leeks |
| 36987-1605 | Leeks | Leeks |
Trademark Results [Leeks]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 LEEKS 77701587 3861632 Live/Registered |
Lee, KengSang 2009-03-28 |
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