# Albuterol Sulfate

NDC: 64980-643
Generic name: Albuterol Sulfate
Labeler / Manufacturer: Rising Pharma Holdings, Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: RESPIRATORY (INHALATION)
Marketing started: 20250414

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:"64980-643"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64980-643
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=32474c0e-af35-69d1-e063-6394a90a53c6