What is NDC 68475-010?

68475-010 is the product NDC for Sevelamer carbonate, Sevelamer carbonate 800 mg/1 tablet, film coated, listed with the FDA by Navinta LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.

Navinta LLC, NDC labeler code 68475. 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 carbonate?

47 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Sevelamer carbonate NDC 68475-010 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68475-010Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68475-0010Add 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
68475-010-01	6847500100168475001001	30 TABLET, FILM COATED in 1 BOTTLE (68475-010-01)Marketed from Nov 1, 2025
68475-010-02	6847500100268475001002	270 TABLET, FILM COATED in 1 BOTTLE (68475-010-02)Marketed from Nov 1, 2025
68475-010-03	6847500100368475001003	180 TABLET, FILM COATED in 1 BOTTLE (68475-010-03)Marketed from Jan 2, 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): Sevelamer carbonate
Generic name (nonproprietary): sevelamer carbonate
Active ingredients: Sevelamer carbonate — 800 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Navinta LLCNDC labeler code 68475
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 219931
Marketing start: Nov 1, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 68475-010_d3c74ca1-7175-40a4-b96f-f864b7f47846SPL ID d3c74ca1-7175-40a4-b96f-f864b7f47846SPL set ID d2f0c283-3e9d-41db-bd4d-83bd21f2a019RxCUI 749206UNII 9YCX42I8IUUPC 0368475010017, 0368475010024, 0368475010031
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

N468475001001 followed by a unit qualifier and the quantity

Package 68475-0010-01. 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 Jan 1, 2026.

Indications (excerpt from the label)

Sevelamer carbonate tablets are indicated for the control of serum phosphorus in adults and children 6 years of age and older with chronic kidney disease (CKD) on dialysis. Sevelamer carbonate tablets are a phosphate binder indicated for the control of serum phosphorus in adults and children 6 years of age and older with chronic kidney disease on dialysis.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68475-010

What is NDC 68475-010?: 68475-010 is the product NDC for Sevelamer carbonate, Sevelamer carbonate 800 mg/1 tablet, film coated, listed with the FDA by Navinta LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Sevelamer carbonate.
What is the active ingredient?: Sevelamer carbonate.
Who is the labeler?: Navinta LLC, NDC labeler code 68475. 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 carbonate?: 47 other product NDCs are listed under this name. See all Sevelamer carbonate 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 carbonate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Sevelamer Carbonate	Sevelamer carbonate 800 mg/1	Tablet, Film coatedOral	INSIGNAMEDEX LLC	87367-266	87367-0266-12
Sevelamer Carbonate	Sevelamer carbonate 800 mg/1	Tablet, Film coatedOral	Marp Pharma	85898-101	85898-0101-27
Sevelamer carbonate	Sevelamer carbonate 800 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	70710-2170	70710-2170-0370710-2170-0770710-2170-08
Sevelamer Carbonate	Sevelamer carbonate 800 mg/1	TabletOral	AiPing Pharmaceutical, Inc.	11788-116	11788-0116-07
Sevelamer Carbonate	Sevelamer carbonate 800 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-562	72789-0562-94
Sevelamer Carbonate	Sevelamer carbonate 800 mg/1	Tablet, Film coatedOral	AvKARE	73190-014	73190-0014-27
Sevelamer Carbonate	Sevelamer carbonate 800 mg/1	Tablet, Film coatedOral	Westminster Pharmaceuticals, LLC	69367-423	69367-0423-27
Sevelamer Carbonate	Sevelamer carbonate 800 mg/1	Tablet, Film coatedOral	Shandong Xinhua Pharmaceutical Co., Ltd.	58624-5001	58624-5001-0258624-5001-04
Sevelamer Carbonate	Sevelamer carbonate .8 g/1	Powder, For suspensionOral	NorthStar RxLLC	72603-398	72603-0398-02
Sevelamer Carbonate	Sevelamer carbonate 800 mg/1	TabletOral	Strides Pharma Science Limited	64380-872	64380-0872-0464380-0872-67

All 48 Sevelamer carbonate NDCs

Other NDCs under ANDA 219931

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

FDA NDC Directory listings under ANDA 219931
Product	Strength	Form · route	Labeler	Product NDC
Sevelamer carbonate	Sevelamer carbonate 800 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	70710-2170