# Levalbuterol

NDC: 76204-900
Generic name: Levalbuterol Hydrochloride
Labeler / Manufacturer: Ritedose Pharmaceuticals, 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: 1.25 mg/3mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76204-900"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76204-900
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d6998949-e1cb-4c86-a480-c0dfd9cb75b5