# Albuterol Sulfate

NDC: 0487-9501
Generic name: Albuterol Sulfate
Labeler / Manufacturer: Nephron Pharmaceuticals Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: RESPIRATORY (INHALATION)
Marketing started: 19970917

FDA application: ANDA074880

## Active ingredients

- ALBUTEROL SULFATE: 2.5 mg/3mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0487-9501"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0487-9501
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=574824f3-51cc-4b94-9c10-e3204d8b19f8