# albuterol sulfate

NDC: 53489-176
Generic name: albuterol sulfate
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19891205

FDA application: ANDA072637

## Active ingredients

- ALBUTEROL SULFATE: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"53489-176"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=53489-176
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=87b8cd3c-2849-4b50-b63e-9ea379165c07