# Levalbuterol

NDC: 0093-4145
Generic name: Levalbuterol
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: RESPIRATORY (INHALATION)
Marketing started: 20130429

FDA application: ANDA090297

## Active ingredients

- LEVALBUTEROL HYDROCHLORIDE: .31 mg/3mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-4145"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-4145
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f3ce78d9-e923-400e-b3cd-3e6124ac7f6d