# Levalbuterol

NDC: 0115-9931
Generic name: Levalbuterol Hydrochloride
Labeler / Manufacturer: Amneal Pharmaceuticals of New York LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: RESPIRATORY (INHALATION)
Marketing started: 20160322

FDA application: ANDA203653

## Active ingredients

- LEVALBUTEROL HYDROCHLORIDE: .63 mg/3mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0115-9931"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0115-9931
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e5c8368a-49f9-45cf-9d42-a871f005edb9