NDC codes

FDA NDC Directory
Product NDC (as listed)70748-173Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70748-0173Add 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
70748-173-2670748017326180 TABLET in 1 BOTTLE (70748-173-26)Marketed from Feb 25, 2022

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)
Sevelamer hydrochloride
Generic name (nonproprietary)
sevelamer hydrochloride
Active ingredients
Sevelamer hydrochloride — 800 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Lupin Pharmaceuticals, Inc.NDC labeler code 70748
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213145
Marketing start
Listing expires
Other FDA classes
Phosphate Chelating Activity (Mechanism)
Identifiers
Product ID 70748-173_cc130cfa-f3e5-460d-92a8-69cc0f958dd2SPL ID cc130cfa-f3e5-460d-92a8-69cc0f958dd2SPL set ID a56c857e-bc39-484c-908d-f5957857efbbRxCUI 857224UNII GLS2PGI8QG
Pharmacologic class
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 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

N470748017326 followed by a unit qualifier and the quantity

Package 70748-0173-26. 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)

Sevelamer hydrochloride tablets are indicated for the control of serum phosphorus in patients with chronic kidney disease (CKD) on dialysis. The safety and efficacy of sevelamer hydrochloride tablets in CKD patients who are not on dialysis have not been studied. Sevelamer hydrochloride tablets are a phosphate binder indicated for the control of serum phosphorus in patients with chronic kidney disease on dialysis. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70748-173

What is NDC 70748-173?
70748-173 is the product NDC for Sevelamer hydrochloride, Sevelamer hydrochloride 800 mg/1 tablet, listed with the FDA by Lupin Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Sevelamer hydrochloride.
What is the active ingredient?
Sevelamer hydrochloride.
Who is the labeler?
Lupin Pharmaceuticals, Inc., NDC labeler code 70748. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sevelamer hydrochloride?
12 other product NDCs are listed under this name. See all Sevelamer hydrochloride NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Sevelamer hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Sevelamer HydrochlorideSevelamer hydrochloride 800 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.70710-205870710-2058-08
sevelamer hydrochlorideSevelamer hydrochloride 800 mg/1Tablet, Film coatedParenteralCardinal Health 107, LLC55154-264755154-2647-00
sevelamer hydrochlorideSevelamer hydrochloride 800 mg/1Tablet, Film coatedParenteralMajor Pharmaceuticals0904-720900904-7209-06
Sevelamer HydrochlorideSevelamer hydrochloride 400 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-08759651-0087-36
Sevelamer HydrochlorideSevelamer hydrochloride 800 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-08859651-0088-18
Sevelamer HydrochlorideSevelamer hydrochloride 400 mg/1Tablet, Film coatedOralMacleods Pharmaceuticals Limited33342-24133342-0241-65
Sevelamer HydrochlorideSevelamer hydrochloride 800 mg/1Tablet, Film coatedOralMacleods Pharmaceuticals Limited33342-24233342-0242-0733342-0242-57
Sevelamer HydrochlorideSevelamer hydrochloride 400 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-250072162-2500-02
Sevelamer HydrochlorideSevelamer hydrochloride 800 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-250172162-2501-02
Sevelamer HydrochlorideSevelamer hydrochloride 800 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-44960687-0449-01

All 13 Sevelamer hydrochloride NDCs

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