# Albuterol Sulfate

NDC: 0487-0301
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: 20100331

FDA application: ANDA076355

## Active ingredients

- ALBUTEROL SULFATE: .63 mg/3mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0487-0301"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0487-0301
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=285a656c-f77f-4e77-b0a8-a0e9c901803f