Prescription drug · ANDA
Sevelamer Hydrochloride NDC 72162-2500
Sevelamer hydrochloride 400 mg/1 · Tablet, Film coated · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72162-2500-2 | 72162250002 | 360 TABLET, FILM COATED in 1 BOTTLE (72162-2500-2)Marketed from May 15, 2025 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 — 400 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Bryant Ranch PrepackNDC labeler code 72162
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 206883
- Marketing start
- Listing expires
- Other FDA classes
- Phosphate Chelating Activity (Mechanism)
- Identifiers
- Product ID 72162-2500_3533646c-b24d-d606-e063-6394a90a5a0bSPL ID 3533646c-b24d-d606-e063-6394a90a5a0bSPL set ID 35337152-9b92-40c0-e063-6294a90a8dd5RxCUI 857216UNII 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
N472162250002followed by a unit qualifier and the quantityPackage 72162-2500-02. 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.
About NDC 72162-2500
- What is NDC 72162-2500?
- 72162-2500 is the product NDC for Sevelamer Hydrochloride, Sevelamer hydrochloride 400 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. 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?
- Bryant Ranch Prepack, NDC labeler code 72162. 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.
Related NDCs: other Sevelamer Hydrochloride products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Sevelamer Hydrochloride | Sevelamer hydrochloride 800 mg/1 | Tablet, Film coatedOral | Zydus Pharmaceuticals USA Inc. | 70710-2058 | 70710-2058-08 |
| sevelamer hydrochloride | Sevelamer hydrochloride 800 mg/1 | Tablet, Film coatedParenteral | Cardinal Health 107, LLC | 55154-2647 | 55154-2647-00 |
| sevelamer hydrochloride | Sevelamer hydrochloride 800 mg/1 | Tablet, Film coatedParenteral | Major Pharmaceuticals | 0904-7209 | 00904-7209-06 |
| Sevelamer Hydrochloride | Sevelamer hydrochloride 400 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 59651-087 | 59651-0087-36 |
| Sevelamer Hydrochloride | Sevelamer hydrochloride 800 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 59651-088 | 59651-0088-18 |
| Sevelamer Hydrochloride | Sevelamer hydrochloride 800 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 72162-2501 | 72162-2501-02 |
| Sevelamer Hydrochloride | Sevelamer hydrochloride 400 mg/1 | Tablet, Film coatedOral | Macleods Pharmaceuticals Limited | 33342-241 | 33342-0241-65 |
| Sevelamer Hydrochloride | Sevelamer hydrochloride 800 mg/1 | Tablet, Film coatedOral | Macleods Pharmaceuticals Limited | 33342-242 | 33342-0242-0733342-0242-57 |
| Sevelamer hydrochloride | Sevelamer hydrochloride 800 mg/1 | TabletOral | Lupin Pharmaceuticals, Inc. | 70748-173 | 70748-0173-26 |
| Sevelamer Hydrochloride | Sevelamer hydrochloride 800 mg/1 | Tablet, Film coatedOral | American Health Packaging | 60687-449 | 60687-0449-01 |
Other NDCs under ANDA 206883
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Sevelamer Hydrochloride | Sevelamer hydrochloride 800 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 72162-2501 |
| Sevelamer Hydrochloride | Sevelamer hydrochloride 400 mg/1 | Tablet, Film coatedOral | Macleods Pharmaceuticals Limited | 33342-241 |
| Sevelamer Hydrochloride | Sevelamer hydrochloride 800 mg/1 | Tablet, Film coatedOral | Macleods Pharmaceuticals Limited | 33342-242 |