Calcium Gluconate NDC 70069-728

NDC codes

FDA NDC Directory

Product NDC (as listed)70069-728Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70069-0728Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
70069-728-10	70069072810	10 VIAL, PLASTIC in 1 CARTON (70069-728-10) / 100 mL in 1 VIAL, PLASTICMarketed from Mar 27, 2024
70069-728-20	70069072820	20 VIAL, PLASTIC in 1 CARTON (70069-728-20) / 100 mL in 1 VIAL, PLASTIC (70069-728-01)Marketed from Oct 20, 2023

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Calcium Gluconate
Generic name (nonproprietary): calcium gluconate
Active ingredients: Calcium gluconate monohydrate — 98 mg/mL
Dosage form: Injection, Solution
Route: Intravenous
Labeler: Somerset Therapeutics, LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217689
Marketing start: Oct 20, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 70069-728_42dd49af-172b-4202-ab5c-442fa942a491SPL ID 42dd49af-172b-4202-ab5c-442fa942a491SPL set ID fb40eba7-04e5-40dc-8a95-5f45e7bd70bcRxCUI 197435, 1668248UNII CZN0MI5R31UPC 0370069727102, 0370069728017, 0370069727010, 0370069728109
Pharmacologic class: Blood Coagulation Factor; Phosphate Binder

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N470069072810 followed by a unit qualifier and the quantity

Package 70069-0728-10. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Feb 6, 2025.

Indications (excerpt from the label)

Calcium gluconate injection is indicated for pediatric and adult patients for the treatment of acute symptomatic hypocalcemia. Limitations of Use The safety of calcium gluconate injection for long term use has not been established. Calcium gluconate injection is a form of calcium indicated for pediatric and adult patients for the treatment of acute symptomatic hypocalcemia. (1) Limitations of Use: The safety of calcium gluconate injection for long term use has not been established. (1)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 217689

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 217689
Product	Strength	Form · route	Labeler	Product NDC
Calcium Gluconate	Calcium gluconate monohydrate 98 mg/mL	Injection, SolutionIntravenous	Somerset Therapeutics, LLC	70069-727