Sodium Bicarbonate NDC 64980-528

NDC codes

FDA NDC Directory

Product NDC (as listed)64980-528Labeler and product segments. Claims need a package NDC.

Product NDC at billing width64980-0528Add 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
64980-528-10	64980052810	1000 TABLET in 1 BOTTLE (64980-528-10)Marketed from Jul 20, 2020

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 — 650 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Rising Pharma Holdings, Inc.
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M001.30
Marketing start: Jul 20, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Alkalinizing Activity (Mechanism)
Identifiers: Product ID 64980-528_2dcd3695-0d50-4ff4-9c9c-171b351156f4SPL ID 2dcd3695-0d50-4ff4-9c9c-171b351156f4SPL set ID f5a90c33-f29d-4d4b-b5e6-0b3c2514ce3eRxCUI 198861UNII 8MDF5V39QO

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 HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N464980052810 followed by a unit qualifier and the quantity

Package 64980-0528-10. 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 Nov 1, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

Uses: relieves • acid indigestion • heartburn • sour stomach • upset stomach associated with these symptoms

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)