# Albuterol Sulfate

NDC: 64980-642
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: ANDA075664

## Active ingredients

- ALBUTEROL SULFATE: 2.5 mg/.5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"64980-642"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64980-642
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3236f82c-14e9-dfd4-e063-6294a90ac43d