NDC 36987-2988
White Pine
White Pine
White Pine 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 Pinus Strobus Pollen.
| Product ID | 36987-2988_69cd05e6-a993-428b-9b0c-0235126ba63b |
| NDC | 36987-2988 |
| Product Type | Human Prescription Drug |
| Proprietary Name | White Pine |
| Generic Name | White Pine |
| 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 | PINUS STROBUS POLLEN |
| Active Ingredient Strength | 0 g/mL |
| Pharm Classes | Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 36987-2988-2
10 mL in 1 VIAL, MULTI-DOSE (36987-2988-2)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 36987-2988-4 [36987298804]
White Pine 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 36987-2988-3 [36987298803]
White Pine 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 36987-2988-1 [36987298801]
White Pine 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 36987-2988-2 [36987298802]
White Pine 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 |
|---|---|
| PINUS STROBUS POLLEN | .1 g/mL |
OpenFDA Data
Pharmacological Class
- Non-Standardized Pollen Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Increased IgG Production [PE]
- Pollen [CS]
- Allergens [CS]
NDC Crossover Matching brand name "White Pine" or generic name "White Pine"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 36987-2981 | White Pine | White Pine |
| 36987-2982 | White Pine | White Pine |
| 36987-2983 | White Pine | White Pine |
| 36987-2984 | White Pine | White Pine |
| 36987-2985 | White Pine | White Pine |
| 36987-2986 | White Pine | White Pine |
| 36987-2987 | White Pine | White Pine |
| 36987-2988 | White Pine | White Pine |
| 0268-6772 | BETULA LENTA POLLEN | White Pine |
| 0268-6651 | PINUS STROBUS POLLEN | White Pine |
Trademark Results [White Pine]
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.