# Albuterol

NDC: 69238-1344
Generic name: Albuterol
Labeler / Manufacturer: Amneal Pharmaceuticals NY LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180524

FDA application: ANDA208804

## 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:"69238-1344"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69238-1344
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=230d66fc-f62c-42a6-adb3-0a0f879c8ad4