# Bumetanide

NDC: 69238-1489
Generic name: Bumetanide
Labeler / Manufacturer: Amneal Pharmaceuticals NY LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20171018

FDA application: ANDA209724

## Active ingredients

- BUMETANIDE: .5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69238-1489"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69238-1489
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9188ab17-8539-48a5-905f-ad35ab5a0b93