NDC 36987-1320
Date
Date
Date 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 Date.
| Product ID | 36987-1320_20425e8b-8db3-4a2b-813b-7e3e1bc1c4e6 |
| NDC | 36987-1320 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Date |
| Generic Name | Date |
| 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 | DATE |
| 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],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Fruit Proteins [EXT] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 36987-1320-4
50 mL in 1 VIAL, MULTI-DOSE (36987-1320-4)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 36987-1320-2 [36987132002]
Date 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 36987-1320-4 [36987132004]
Date 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 36987-1320-1 [36987132001]
Date 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 36987-1320-3 [36987132003]
Date 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 |
|---|---|
| DATE | .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]
- Allergens [CS]
- Dietary Proteins [CS]
- Plant Proteins [CS]
- Fruit Proteins [EXT]
NDC Crossover Matching brand name "Date" or generic name "Date"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 36987-1318 | Date | Date |
| 36987-1319 | Date | Date |
| 36987-1320 | Date | Date |
| 36987-1321 | Date | Date |
| 49288-0161 | Date | Date |
| 54575-387 | DATE | date |
Trademark Results [Date]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 DATE 79248144 not registered Live/Pending |
DATE S.r.l. 2018-07-19 |
 DATE 79211698 5393625 Live/Registered |
DNV GL AS 2016-11-24 |
 DATE 78209603 2860109 Dead/Cancelled |
SYTEXX GmbH 2003-01-31 |
 DATE 76152748 not registered Dead/Abandoned |
TRI-COASTAL DESIGN GROUP, INC. 2000-10-25 |
 DATE 74716599 not registered Dead/Abandoned |
Bull HN Information Systems Inc. 1995-08-16 |
 DATE 74523314 not registered Dead/Abandoned |
Bull HN Information Systems, Inc. 1994-05-02 |
 DATE 73423825 1305954 Dead/Cancelled |
Lucky, Ltd. 1983-04-29 |
 DATE 73381982 not registered Dead/Abandoned |
LUCKY, LTD. 1982-08-26 |
 DATE 73201779 1135425 Dead/Cancelled |
INTERNATIONAL PLAYTEX, INC. 1979-01-29 |
 DATE 72115313 0735436 Dead/Cancelled |
Dr. Pepper Company 1961-03-10 |
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