United States · FDA National Drug Code directory
Succinylcholine Chloride
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
- 70069-783_a8e53864-45c5-4118-960f-70af666c62d9
- Product NDC
- 70069-783
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Succinylcholine Chloride
- Labeler
- Somerset Therapeutics, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230530
- Source listing expiry
- 20271231
Source-listed ingredients
- SUCCINYLCHOLINE CHLORIDE — 20 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 CARTON (70069-783-10) / 10 mL in 1 VIAL · 70069-783-10
- 25 VIAL in 1 CARTON (70069-783-25) / 10 mL in 1 VIAL · 70069-783-25
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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