NDC 49288-0080
White Birch
White Birch
White Birch 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 Betula Populifolia Pollen.
| Product ID | 49288-0080_13c9eea1-38b5-472b-b735-a814ca886718 |
| NDC | 49288-0080 |
| Product Type | Human Prescription Drug |
| Proprietary Name | White Birch |
| Generic Name | White Birch |
| 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 | BETULA POPULIFOLIA 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 49288-0080-5
50 mL in 1 VIAL, MULTI-DOSE (49288-0080-5)
| Marketing Start Date | 1974-03-23 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 49288-0080-4 [49288008004]
White Birch 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 49288-0080-1 [49288008001]
White Birch 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 49288-0080-2 [49288008002]
White Birch 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 49288-0080-3 [49288008003]
White Birch 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 49288-0080-5 [49288008005]
White Birch 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 |
|---|---|
| BETULA POPULIFOLIA 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 Birch" or generic name "White Birch"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 36987-2549 | White Birch | White Birch |
| 36987-2550 | White Birch | White Birch |
| 36987-2551 | White Birch | White Birch |
| 36987-2552 | White Birch | White Birch |
| 36987-2553 | White Birch | White Birch |
| 36987-2554 | White Birch | White Birch |
| 36987-2555 | White Birch | White Birch |
| 36987-2556 | White Birch | White Birch |
| 49288-0080 | White Birch | White Birch |
| 0268-6610 | BETULA LENTA POLLEN | White Birch |
| 0268-6688 | BETULA LENTA POLLEN | White Birch |
Trademark Results [White Birch]
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.