# Albuterol Sulfate

NDC: 0054-0742
Generic name: Albuterol Sulfate
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: AEROSOL, METERED
Routes: RESPIRATORY (INHALATION)
Marketing started: 20211130

FDA application: ANDA207085

## 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:"0054-0742"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0054-0742
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6c64ab5d-f8a2-440a-a929-cb8188d0e8b4