# ALBUTEROL SULFATE

NDC: 81894-104
Generic name: ALBUTEROL SULFATE
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: 20171017

FDA application: ANDA206224

## Active ingredients

- ALBUTEROL SULFATE: .83 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"81894-104"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81894-104
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1810ff8e-d505-bf9c-e063-6394a90a6540