United States · FDA National Drug Code directory
Sodium Nitroprusside
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
- 75907-290_b246076f-49e6-6a0d-e065-9b3f853adb2d
- Product NDC
- 75907-290
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Sodium Nitroprusside
- Labeler
- Dr.Reddy's Laboratories Inc.,
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251201
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM NITROPRUSSIDE — 50 mg/2mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, SINGLE-DOSE in 1 CARTON (75907-290-11) / 2 mL in 1 VIAL, SINGLE-DOSE · 75907-290-11
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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