# Albuterol Sulfate

NDC: 70518-3560
Generic name: albuterol sulfate
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: RESPIRATORY (INHALATION)
Marketing started: 20221019

FDA application: ANDA207857

## Active ingredients

- ALBUTEROL SULFATE: .83 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-3560"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-3560
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0f9bf2c8-55c0-4b4d-97de-d6c7220c3862