# Levalbuterol

NDC: 0378-9690
Generic name: Levalbuterol
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: RESPIRATORY (INHALATION)
Marketing started: 20180723

FDA application: ANDA203653

## Active ingredients

- LEVALBUTEROL HYDROCHLORIDE: .31 mg/3mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-9690"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-9690
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5b4fa89e-aa46-4504-a275-246f3b4df1df