NDC 36987-1456
Lentil
Lentil
Lentil 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 Lentil.
| Product ID | 36987-1456_20425e8b-8db3-4a2b-813b-7e3e1bc1c4e6 |
| NDC | 36987-1456 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Lentil |
| Generic Name | Lentil |
| 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 | LENTIL |
| Active Ingredient Strength | 0 g/mL |
| Pharm Classes | Non-Standardized Food Allergenic Extract [EPC],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Dietary Proteins [CS],Plant Proteins [CS],Allergens [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 36987-1456-2
10 mL in 1 VIAL, MULTI-DOSE (36987-1456-2)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 36987-1456-3 [36987145603]
Lentil 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 36987-1456-2 [36987145602]
Lentil 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 36987-1456-4 [36987145604]
Lentil 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 36987-1456-1 [36987145601]
Lentil 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 |
|---|---|
| LENTIL | .1 g/mL |
OpenFDA Data
Pharmacological Class
- Non-Standardized Food Allergenic Extract [EPC]
- Non-Standardized Plant Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Dietary Proteins [CS]
- Plant Proteins [CS]
- Allergens [CS]
NDC Crossover Matching brand name "Lentil" or generic name "Lentil"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 36987-1454 | Lentil | Lentil |
| 36987-1455 | Lentil | Lentil |
| 36987-1456 | Lentil | Lentil |
| 36987-1457 | Lentil | Lentil |
| 49288-0290 | Lentil | Lentil |
Trademark Results [Lentil]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 LENTIL 88295333 not registered Live/Pending |
YGreen, Inc. 2019-02-09 |
 LENTIL 75633022 not registered Dead/Abandoned |
OroAmerica, Inc. 1999-02-03 |
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