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Sevelamer carbonate - Medication Information

Product NDC Code 70771-1520
Drug Name

Sevelamer carbonate

Type Generic
Pharm Class Phosphate Binder [EPC],
Phosphate Chelating Activity [MoA]
Active Ingredients
Sevelamer carbonate 800 mg/1
Route ORAL
Dosage Form TABLET, FILM COATED
RxCUI drug identifier 749206
Application Number ANDA207759
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
70771-1520-0 1000 tablet, film coated in 1 bottle (70771-1520-0)
70771-1520-4 10 blister pack in 1 carton (70771-1520-4) / 10 tablet, film coated in 1 blister pack (70771-1520-2)
70771-1520-8 270 tablet, film coated in 1 bottle (70771-1520-8)
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Spl product data elements

Usually a list of ingredients in a drug product.
Sevelamer carbonate Sevelamer carbonate SEVELAMER CARBONATE SEVELAMER CASTOR OIL CROSPOVIDONE (15 MPA.S AT 5%) DIBUTYL SEBACATE FERROSOFERRIC OXIDE HYPROMELLOSE 2910 (15 MPA.S) HYPROMELLOSE 2910 (5 MPA.S) HYPROMELLOSE 2910 (50 MPA.S) HYPROMELLOSE 2910 (6 MPA.S) LACTOSE MONOHYDRATE MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POLYVINYL ALCOHOL, UNSPECIFIED POVIDONE K90 PROPYLENE GLYCOL SHELLAC SILICON DIOXIDE TRIACETIN WATER off-white to pale yellow MODIFIED CAPSULE 824

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1520-8 Sevelamer Tablets, 800 mg 270 Tablets Rx only label

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API