# SODIUM NITROPRUSSIDE

NDC: 42571-265
Generic name: SODIUM NITROPRUSSIDE
Labeler / Manufacturer: Micro Labs Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20171230

FDA application: ANDA209352

## Active ingredients

- SODIUM NITROPRUSSIDE: 50 mg/2mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42571-265"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42571-265
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5a599880-c133-44ef-a9f2-bd1b681563be