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
- 84897-013_7d9f7399-2dfe-4c5a-9946-f011d8a8c6fe
- Product NDC
- 84897-013
- Form
- INJECTION, SOLUTION
- Composition / generic term
- CUPRIC CHLORIDE
- Labeler
- Renova Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260507
- Source listing expiry
- 20271231
Source-listed ingredients
- CUPRIC CHLORIDE — .4 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL, SINGLE-DOSE in 1 PACKAGE (84897-013-25) / 10 mL in 1 VIAL, SINGLE-DOSE (84897-013-01) · 84897-013-25
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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