# CENTER-AL - AMBROSIA ARTEMISIIFOLIA POLLEN

NDC: 0268-0156
Generic name: AMBROSIA ARTEMISIIFOLIA POLLEN
Labeler / Manufacturer: ALK-Abello, Inc.
Product type: NON-STANDARDIZED ALLERGENIC
Marketing category: Biologic License Application
Dosage form: INJECTION, SUSPENSION
Routes: SUBCUTANEOUS
Marketing started: 19750115

FDA application: BLA103753

## Active ingredients

- AMBROSIA ARTEMISIIFOLIA POLLEN: 20000 [PNU]/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0268-0156"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0268-0156