United States · FDA National Drug Code directory
Calcium Gluconate
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
- 63323-360_661fc3fe-30e4-4d3e-a7a0-7405bfabe79f
- Product NDC
- 63323-360
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Calcium Gluconate
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20170615
- Source listing expiry
- 20271231
Source-listed ingredients
- CALCIUM GLUCONATE MONOHYDRATE — 100 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL, PLASTIC in 1 TRAY (63323-360-19) / 10 mL in 1 VIAL, PLASTIC (63323-360-01) · 63323-360-19
- 25 VIAL, PLASTIC in 1 TRAY (63323-360-59) / 50 mL in 1 VIAL, PLASTIC (63323-360-03) · 63323-360-59
- 20 VIAL, PLASTIC in 1 TRAY (63323-360-61) / 100 mL in 1 VIAL, PLASTIC (63323-360-05) · 63323-360-61
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 →