What is NDC 0955-1052?

0955-1052 is the product NDC for Sevelamer Carbonate, Sevelamer carbonate .8 g/1 powder, for suspension, listed with the FDA by Sanofi-Aventis U.S. LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Sanofi-Aventis U.S. LLC, NDC labeler code 0955. 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 0955-1052 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0955-1052Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00955-1052Add 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
0955-1052-90	0095510529000955105290	90 PACKET in 1 BOX (0955-1052-90) / 1 POWDER, FOR SUSPENSION in 1 PACKET (0955-1052-01)Marketed from Jan 1, 2018

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 — .8 g/1
Dosage form: Powder, For suspension
Route: Oral
Labeler: Sanofi-Aventis U.S. LLCNDC labeler code 0955
Product type: Prescription drug
Marketing category: NDA authorized genericApplication NDA 022318
Marketing start: Jan 1, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 0955-1052_42bdb389-5550-487c-aed2-c4e3afd239c8SPL ID 42bdb389-5550-487c-aed2-c4e3afd239c8SPL set ID 3abc32fe-1bfc-4759-8f7c-36095e221b06RxCUI 749206, 861370, 861375UNII 9YCX42I8IU
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

N400955105290 followed by a unit qualifier and the quantity

Package 00955-1052-90. 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 25, 2025.

Indications (excerpt from the label)

Sevelamer carbonate is 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 is 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. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0955-1052

What is NDC 0955-1052?: 0955-1052 is the product NDC for Sevelamer Carbonate, Sevelamer carbonate .8 g/1 powder, for suspension, listed with the FDA by Sanofi-Aventis U.S. LLC. It has 1 package NDC, 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?: Sanofi-Aventis U.S. LLC, NDC labeler code 0955. 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	Navinta LLC	68475-010	68475-0010-0168475-0010-0268475-0010-03
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

All 48 Sevelamer Carbonate NDCs

Other NDCs under NDA 022318

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

FDA NDC Directory listings under NDA 022318
Product	Strength	Form · route	Labeler	Product NDC
Renvelasevelamer carbonate	Sevelamer carbonate 2400 mg/1	Powder, For suspensionOral	Genzyme Corporation	58468-0131
Renvelasevelamer carbonate	Sevelamer carbonate 800 mg/1	Powder, For suspensionOral	Genzyme Corporation	58468-0132
Sevelamer Carbonate	Sevelamer carbonate 2.4 g/1	Powder, For suspensionOral	Sanofi-Aventis U.S. LLC	0955-1054