NDC 49288-0016
White Alder
White Alder
White Alder 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 Alnus Rhombifolia Pollen.
| Product ID | 49288-0016_13c9eea1-38b5-472b-b735-a814ca886718 |
| NDC | 49288-0016 |
| Product Type | Human Prescription Drug |
| Proprietary Name | White Alder |
| Generic Name | White Alder |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRADERMAL; SUBCUTANEOUS |
| Marketing Start Date | 1974-03-23 |
| Marketing Category | BLA / BLA |
| Application Number | BLA102223 |
| Labeler Name | Antigen Laboratories, Inc. |
| Substance Name | ALNUS RHOMBIFOLIA 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 49288-0016-4
30 mL in 1 VIAL, MULTI-DOSE (49288-0016-4)
| Marketing Start Date | 1974-03-23 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 49288-0016-1 [49288001601]
White Alder INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0016-5 [49288001605]
White Alder INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0016-3 [49288001603]
White Alder INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0016-4 [49288001604]
White Alder INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
NDC 49288-0016-2 [49288001602]
White Alder INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102223 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-03-23 |
| Inactivation Date | 2019-10-21 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| ALNUS RHOMBIFOLIA 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 "White Alder" or generic name "White Alder"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 36987-2469 | White Alder | White Alder |
| 36987-2470 | White Alder | White Alder |
| 36987-2471 | White Alder | White Alder |
| 36987-2472 | White Alder | White Alder |
| 36987-2473 | White Alder | White Alder |
| 36987-2474 | White Alder | White Alder |
| 36987-2475 | White Alder | White Alder |
| 36987-2476 | White Alder | White Alder |
| 49288-0016 | White Alder | White Alder |
| 0268-6601 | ALNUS INCANA SSP RUGOSA POLLEN | White Alder |
| 0268-6678 | ALNUS INCANA SSP RUGOSA POLLEN | White Alder |
Trademark Results [White Alder]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 WHITE ALDER 85819481 4467720 Live/Registered |
Lyrical Foods, Inc. 2013-01-09 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.