# ALBUTEROL SULFATE

NDC: 50090-5735
Generic name: albuterol sulfate
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INHALANT
Routes: RESPIRATORY (INHALATION)
Marketing started: 20200408

FDA application: ANDA209959

## Active ingredients

- ALBUTEROL SULFATE: 90 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-5735"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-5735
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7ad17b39-d2de-4108-abbf-cedd650c8edd