# Levalbuterol

NDC: 0378-6993
Generic name: levalbuterol
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION, CONCENTRATE
Routes: RESPIRATORY (INHALATION)
Marketing started: 20090828

FDA application: ANDA078309

## Active ingredients

- LEVALBUTEROL HYDROCHLORIDE: 1.25 mg/.5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-6993"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-6993
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=206bbdec-04f0-40e3-a259-32fc6bce20d8