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: 67457-839_c4d84a94-85c2-4073-b1aa-c4f4b21a500a
Product NDC: 67457-839
Form: INJECTION, SOLUTION, CONCENTRATE
Composition / generic term: Sodium nitroprusside
Labeler: Mylan Institutional LLC
Marketing category: ANDA
Marketing start / end (source format): 20180810
Source listing expiry: 20271231

Source-listed ingredients

SODIUM NITROPRUSSIDE — 25 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

1 VIAL, SINGLE-DOSE in 1 CARTON (67457-839-02) / 2 mL in 1 VIAL, SINGLE-DOSE · 67457-839-02

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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