United States · FDA National Drug Code directory
NIPRIDE RTU
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 51754-1006_ed0040fb-c481-4477-8712-00fa6350cd70
- Product NDC
- 51754-1006
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Sodium Nitroprusside
- Labeler
- EXELA PHARMA SCIENCES, LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20170320
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM NITROPRUSSIDE — .5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 VIAL (51754-1006-1) / 100 mL in 1 VIAL · 51754-1006-1
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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