# Standardized Mite Dermatophagoides pteronyssinus

NDC: 22840-0035
Generic name: Dermatophagoides pteronyssinus
Labeler / Manufacturer: Greer Laboratories, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: CONCENTRATE
Routes: INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Marketing started: 19890627

FDA application: BLA101835

## Active ingredients

- DERMATOPHAGOIDES PTERONYSSINUS: 5000 [AU]/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"22840-0035"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=22840-0035
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9b7f878e-613f-4831-9223-a6a07fb09f1b
