What is NDC 65862-930?

65862-930 is the product NDC for Sevelamer Carbonate, Sevelamer carbonate 800 mg/1 powder, for suspension, listed with the FDA by Aurobindo Pharma Limited. It has 1 package NDC, shown above in 10- and 11-digit form.

Aurobindo Pharma Limited, NDC labeler code 65862. 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 65862-930 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)65862-930Labeler and product segments. Claims need a package NDC.

Product NDC at billing width65862-0930Add 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
65862-930-90	6586209309065862093090	90 POUCH in 1 CARTON (65862-930-90) / 1 POWDER, FOR SUSPENSION in 1 POUCH (65862-930-08)Marketed from Jun 13, 2017

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: Powder, For suspension
Route: Oral
Labeler: Aurobindo Pharma LimitedNDC labeler code 65862
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207624
Marketing start: Jun 13, 2017
Listing expires: Dec 31, 2027
Other FDA classes: Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 65862-930_e8c6db3c-3509-4033-8161-555236328bedSPL ID e8c6db3c-3509-4033-8161-555236328bedSPL set ID ea201bff-cdfb-4304-bdb1-d05c1dac2677RxCUI 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

N465862093090 followed by a unit qualifier and the quantity

Package 65862-0930-90. 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 Dec 8, 2023.

Indications (excerpt from the label)

Sevelamer carbonate for oral suspension 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 for oral suspension 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 65862-930

What is NDC 65862-930?: 65862-930 is the product NDC for Sevelamer Carbonate, Sevelamer carbonate 800 mg/1 powder, for suspension, listed with the FDA by Aurobindo Pharma Limited. 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?: Aurobindo Pharma Limited, NDC labeler code 65862. 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 ANDA 207624

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

FDA NDC Directory listings under ANDA 207624
Product	Strength	Form · route	Labeler	Product NDC
Sevelamer Carbonate	Sevelamer carbonate 2400 mg/1	Powder, For suspensionOral	Aurobindo Pharma Limited	65862-931