Spring Birch Pollen .05 g/mL
Betula fontinalis · INJECTION · Allermed Laboratories, Inc.
Spring Birch Pollen is an injectable medication given under the skin that contains birch pollen extract and is available over-the-counter. This product is typically used for allergen immunotherapy to help reduce allergic reactions to birch pollen.
Key Facts
- Brand Name
- Spring Birch Pollen
- Generic Name
- Betula fontinalis
- NDC Code (Product)
49643-441- Manufacturer
- Allermed Laboratories, Inc.
- Strength
- .05 g/mL
- Dosage Form
- INJECTION
- Route
- CUTANEOUS, INTRADERMAL, SUBCUTANEOUS
- Marketing Status
- Application #
- BLA102211
- Marketing Start
- 03/12/1974
Recall History
No Recall HistoryFrequently Asked Questions
What is Spring Birch Pollen used for?
Spring Birch Pollen is an injectable medication given under the skin that contains birch pollen extract and is available over-the-counter. This product is typically used for allergen immunotherapy to help reduce allergic reactions to birch pollen.
Is Spring Birch Pollen a controlled substance?
Spring Birch Pollen is not classified as a controlled substance by the DEA.
What is the generic name for Spring Birch Pollen?
The generic name for Spring Birch Pollen is Betula fontinalis. There are no other listed brand versions of Betula fontinalis.
What is the NDC code for Spring Birch Pollen .05 g/mL?
The NDC (National Drug Code) for Spring Birch Pollen .05 g/mL is 49643-441, listed by Allermed Laboratories, Inc..
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)