United States · FDA National Drug Code directory
CUPRIC 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
- 51754-0103_18dc9e1c-b9db-4160-96f7-8c4391bcf8c9
- Product NDC
- 51754-0103
- Form
- INJECTION, SOLUTION
- Composition / generic term
- cupric chloride
- Labeler
- Exela Pharma Sciences, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230201
- Source listing expiry
- 20261231
Source-listed ingredients
- CUPRIC CHLORIDE — .4 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, SINGLE-DOSE in 1 CARTON (51754-0103-3) / 10 mL in 1 VIAL, SINGLE-DOSE · 51754-0103-3
- 25 VIAL, SINGLE-DOSE in 1 CARTON (51754-0103-4) / 10 mL in 1 VIAL, SINGLE-DOSE · 51754-0103-4
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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