# Albuterol

NDC: 71205-899
Generic name: albuterol
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180629

FDA application: ANDA207046

## Active ingredients

- ALBUTEROL SULFATE: 4 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-899"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-899
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=895dff1c-d21c-4470-b021-a5b68364c1ec