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
- 80830-2301_0483ece7-d1e5-4787-a73e-1b41c75f26a7
- Product NDC
- 80830-2301
- Form
- INJECTION, SOLUTION
- Composition / generic term
- CUPRIC CHLORIDE
- Labeler
- Amneal Pharmaceuticals Private Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260129
- 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 in 1 CARTON (80830-2301-5) / 10 mL in 1 VIAL (80830-2301-1) · 80830-2301-5
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →