NDC codes

FDA NDC Directory
Product NDC (as listed)64980-729Labeler and product segments. Claims need a package NDC.
Product NDC at billing width64980-0729Add 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 NDC11-digit (billing)PackageCopy
64980-729-016498007290164980072901100 TABLET in 1 BOTTLE (64980-729-01)Marketed from Mar 28, 2026

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)
Phospha 250 Neutral
Generic name (nonproprietary)
dibasic sodium phosphate, monobasic potassium phosphate and monobasic sodium phosphate
Dosage form
Tablet
Route
Oral
Labeler
Rising Pharma Holdings, Inc.NDC labeler code 64980
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 64980-729_f6c34864-dbd6-436e-b1e5-b1feaa61696aSPL ID f6c34864-dbd6-436e-b1e5-b1feaa61696aSPL set ID 9432adfc-6add-4ab4-ae93-2e2daf348be2RxCUI 200251, 656742UNII 22ADO53M6F, 4J9FJ0HL51, 593YOG76RNUPC 0364980729017

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

N464980072901 followed by a unit qualifier and the quantity

Package 64980-0729-01. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE PHOSPHA 250 TM NEUTRAL increases urinary phosphate and pyrophosphate. As a phosphorus supplement, each tablet supplies 25% of the U.S. Recommended Daily Allowance (U.S. RDA) of phosphorus for adults and children over 4 years of age.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 64980-729

What is NDC 64980-729?
64980-729 is the product NDC for Phospha 250 Neutral, Sodium phosphate, Dibasic, Anhydrous 852 mg/1 + 2 more ingredients tablet, listed with the FDA by Rising Pharma Holdings, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Phospha 250 Neutral (Dibasic Sodium Phosphate, Monobasic Potassium Phosphate and Monobasic Sodium Phosphate).
What is the active ingredient?
Sodium phosphate, Dibasic, Anhydrous, Potassium phosphate, Monobasic, Sodium phosphate, Monobasic, Monohydrate.
Who is the labeler?
Rising Pharma Holdings, Inc., NDC labeler code 64980. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Phospha 250 Neutral?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

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