# albuterol sulfate

NDC: 71205-441
Generic name: albuterol sulfate
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: AEROSOL, METERED
Routes: RESPIRATORY (INHALATION)
Marketing started: 20200226

FDA application: ANDA203760

## 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:"71205-441"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-441
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=918551c7-c3c1-43bc-b575-b33fdb4e96fc