# Albuterol sulfate

NDC: 70518-3541
Generic name: Albuterol sulfate
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: AEROSOL, METERED
Routes: RESPIRATORY (INHALATION)
Marketing started: 20220928

FDA application: ANDA209954

## Active ingredients

- ALBUTEROL SULFATE: 90 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-3541"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-3541
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0cfb6c5d-eac2-4a1c-8a0f-6b00e819adda