# Albuterol Sulfate

NDC: 68788-8874
Generic name: Albuterol Sulfate
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INHALANT
Routes: RESPIRATORY (INHALATION)
Marketing started: 20250516

FDA application: ANDA209959

## 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:"68788-8874"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8874
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1c72fd84-7dbc-45d0-ab88-fb4221ce369f