# Albuterol Sulfate

NDC: 71205-641
Generic name: albuterol sulfate
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: RESPIRATORY (INHALATION)
Marketing started: 20210611

FDA application: ANDA207857

## 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:"71205-641"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-641
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a6545fbe-b0a6-41ae-8bb6-91af38410f56