NDC 49288-0411
Eastern White Pine
Eastern White Pine
Eastern White Pine is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Antigen Laboratories, Inc.. The primary component is Pinus Strobus Pollen.
| Product ID | 49288-0411_13c9eea1-38b5-472b-b735-a814ca886718 |
| NDC | 49288-0411 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Eastern White Pine |
| Generic Name | Eastern White Pine |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRADERMAL; SUBCUTANEOUS |
| Marketing Start Date | 1979-09-09 |
| Marketing Category | BLA / BLA |
| Application Number | BLA102223 |
| Labeler Name | Antigen 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 49288-0411-1
2 mL in 1 VIAL, MULTI-DOSE (49288-0411-1)
| Marketing Start Date | 1979-09-09 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 49288-0411-5 [49288041105]
Eastern White Pine INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1979-09-09 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0411-2 [49288041102]
Eastern White Pine INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1979-09-09 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0411-4 [49288041104]
Eastern White Pine INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1979-09-09 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0411-1 [49288041101]
Eastern White Pine INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1979-09-09 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0411-3 [49288041103]
Eastern White Pine INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1979-09-09 |
| Inactivation Date | 2019-10-21 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| PINUS STROBUS POLLEN | .05 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 "Eastern White Pine" or generic name "Eastern White Pine"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 49288-0410 | Eastern White Pine | Eastern White Pine |
| 49288-0411 | Eastern White Pine | Eastern White Pine |
Trademark Results [Eastern White Pine]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 EASTERN WHITE PINE 78427861 not registered Dead/Abandoned |
Timber Trading, Inc. 2004-06-01 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.