# bumetanide

NDC: 68382-526
Generic name: bumetanide
Labeler / Manufacturer: Zydus Pharmaceuticals (USA) Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180501

FDA application: ANDA202900

## Active ingredients

- BUMETANIDE: 1 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68382-526"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68382-526
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=525138cd-832a-41d0-84b0-83921b12bd2a