# Bumetanide

NDC: 68462-470
Generic name: Bumetanide
Labeler / Manufacturer: GLENMARK PHARMACEUTICALS INC., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20230101

FDA application: ANDA216434

## Active ingredients

- BUMETANIDE: .25 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68462-470"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-470
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=680563fe-5d3a-49bc-86a5-740bda2acebe