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
- 68462-789_b2470072-f443-4596-ae33-1b8b0d05bc9d
- Product NDC
- 68462-789
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Calcium Gluconate
- Labeler
- GLENMARK PHARMACEUTICALS INC., USA
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260504
- 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 CARTON (68462-789-25) / 10 mL in 1 VIAL, PLASTIC (68462-789-10) · 68462-789-25
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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