Sodium Bicarbonate NDC 68462-951

NDC codes

FDA NDC Directory

Product NDC (as listed)68462-951Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68462-0951Add 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
68462-951-65	68462095165	25 VIAL in 1 CARTON (68462-951-65) / 50 mL in 1 VIAL (68462-951-50)Marketed from Aug 7, 2025

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): Sodium Bicarbonate
Generic name (nonproprietary): sodium bicarbonate
Active ingredients: Sodium bicarbonate — 84 mg/mL
Dosage form: Injection, Solution
Route: Intravenous
Labeler: Glenmark Pharmaceuticals Inc., USA
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 219701
Marketing start: Aug 7, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Alkalinizing Activity (Mechanism)
Identifiers: Product ID 68462-951_f38d0dfc-9bcc-4224-a202-885c9ad0beaeSPL ID f38d0dfc-9bcc-4224-a202-885c9ad0beaeSPL set ID f38d0dfc-9bcc-4224-a202-885c9ad0beaeRxCUI 1868486UNII 8MDF5V39QOUPC 0368462951507, 0368462951651

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

N468462095165 followed by a unit qualifier and the quantity

Package 68462-0951-65. 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 Nov 20, 2025.

Indications (excerpt from the label)

CONTRAINDICATIONS Sodium bicarbonate injection is contraindicated in patients who are losing chloride by vomiting or from continuous gastrointestinal suction, and in patients receiving diuretics known to produce a hypochloremic alkalosis.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 219701

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

FDA NDC Directory listings under ANDA 219701
Product	Strength	Form · route	Labeler	Product NDC
Sodium Bicarbonate	Sodium bicarbonate 84 mg/mL	Injection, SolutionIntravenous	Medical Purchasing Solutions, LLC.	71872-7376
Sodium Bicarbonate	Sodium bicarbonate 84 mg/mL	Injection, SolutionIntravenous	Anthea Pharma Private Limited	83854-001