# Levalbuterol

NDC: 81894-102
Generic name: Levalbuterol
Labeler / Manufacturer: Luoxin Aurovitas Pharma (Chengdu) Co., Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: RESPIRATORY (INHALATION)
Marketing started: 20161230

FDA application: ANDA207625

## 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:"81894-102"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81894-102
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=29eae75d-93da-7a5a-e063-6394a90ac0c0