# Albuterol Sulfate

NDC: 0378-8270
Generic name: Albuterol Sulfate
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: RESPIRATORY (INHALATION)
Marketing started: 20121015

FDA application: ANDA077839

## Active ingredients

- ALBUTEROL SULFATE: 2.5 mg/3mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-8270"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-8270
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5329614f-ae0b-4854-bb6f-ea0b7dae87c0