Sodium Citrate
Sodium Citrate · TRISODIUM CITRATE DIHYDRATE 230 mg/1 · Tablet, Chewable · Contract Pharmacal Corp.
NDC 10267-4243-01 · 10 TABLET, CHEWABLE in 1 BLISTER PACK · DRUG FOR FURTHER PROCESSING · View full market →
Bulk ingredient — not a finished product
This NDC is a raw material (drug for further processing) sold to drug manufacturers or compounders, not a product pharmacies dispense. Retail pricing, TE codes, fragility scores, and shortage reports don't apply to bulk listings — those attach to finished products made from this ingredient.
Medicare Part D
This is a bulk ingredient, not a dispensable product — it is a raw material sold to manufacturers and compounders, so no plan prices it.
How Part D pricing works →NADAC price per unit
No NADAC pricing on file for this NDC — NADAC covers drugs dispensed by retail community pharmacies.
Supply fragility
Not scored — fragility is computed for NADAC-priced NDCs.
Regulatory
- Application
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- TE code
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- Approval date
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- Patents / exclusivity
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Shortage history
No FDA shortage reports for this drug or its presentations.
Recalls (this NDC)
No enforcement reports list this package NDC.
Manufacturers of Sodium Citrate (Tablet, Chewable)
| Labeler | Strength | First seen | Last seen |
|---|---|---|---|
| Kobayashi Healthcare International, Inc. | TRISODIUM CITRATE DIHYDRATE 230 mg/1 | Jul 15, 2026 | Sep 3, 2026 |
| Contract Pharmacal Corp. | TRISODIUM CITRATE DIHYDRATE 230 mg/1 | Jul 15, 2026 | Sep 2, 2026 |
Roster from daily NDC Directory diffs — first/last seen dates start July 2026.
Cite this page
DrugDashboards, "Sodium Citrate — NDC 10267-4243-01," retrieved September 3, 2026, https://drugdashboards.com/drug/10267424301.
Free to cite with attribution — see how the data is put together.