NDC codes

FDA NDC Directory
Product NDC (as listed)64980-104Labeler and product segments. Claims need a package NDC.
Product NDC at billing width64980-0104Add 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
64980-104-0164980010401100 TABLET in 1 BOTTLE (64980-104-01)Marketed from Jun 28, 2012

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)
Dibasic Sodium Phosphate, Monobasic Potassium Phosphate and Monobasic Sodium Phosphate
Generic name (nonproprietary)
dibasic sodium phosphate, monobasic potassium phosphate and monobasic sodium phosphate
Active ingredients
Sodium phosphate, Dibasic, Anhydrous — 852 mg/1Potassium phosphate, Monobasic — 155 mg/1Sodium phosphate, Monobasic, Monohydrate — 130 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Marketing end
Identifiers
Product ID 64980-104_6e5bf656-cf34-4279-b2f4-7c1893cf7275SPL ID 6e5bf656-cf34-4279-b2f4-7c1893cf7275SPL set ID b01eac95-dbe3-4b21-a922-187e0fc8ad23RxCUI 200251UNII 22ADO53M6F, 4J9FJ0HL51, 593YOG76RNUPC 0364980104012

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

N464980010401 followed by a unit qualifier and the quantity

Package 64980-0104-01. 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)

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