# ALBUTEROL SULFATE

NDC: 81894-106
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: 20200420

FDA application: ANDA211888

## Active ingredients

- ALBUTEROL SULFATE: 1.25 mg/3mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"81894-106"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81894-106
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1d6be2b8-c670-b783-e063-6294a90ae503