sevelamer carbonate

Generic: sevelamer carbonate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sevelamer carbonate
Generic Name sevelamer carbonate
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sevelamer carbonate 800 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-3021
Product ID 71335-3021_5c329e0c-2108-4e78-9cfb-46a153a7319d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206100
Listing Expiration 2026-12-31
Marketing Start 2023-04-19

Pharmacologic Class

Classes
phosphate binder [epc] phosphate chelating activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713353021
Hyphenated Format 71335-3021

Supplemental Identifiers

RxCUI
749206
UNII
9YCX42I8IU

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sevelamer carbonate (source: ndc)
Generic Name sevelamer carbonate (source: ndc)
Application Number ANDA206100 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 800 mg/1
source: ndc
Packaging
  • 50 TABLET, FILM COATED in 1 BOTTLE (71335-3021-1)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-3021-2)
  • 100 TABLET, FILM COATED in 1 BOTTLE (71335-3021-3)
source: ndc

Packages (3)

71335-3021-1 50 TABLET, FILM COATED in 1 BOTTLE (71335-3021-1) 71335-3021-2 90 TABLET, FILM COATED in 1 BOTTLE (71335-3021-2) 71335-3021-3 100 TABLET, FILM COATED in 1 BOTTLE (71335-3021-3)

Ingredients (1)

sevelamer carbonate (800 mg/1)

Linked Drug Pages (1)

Sevelamer Carbonate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5c329e0c-2108-4e78-9cfb-46a153a7319d", "openfda": {"unii": ["9YCX42I8IU"], "rxcui": ["749206"], "spl_set_id": ["26307350-69bb-40c9-9d5b-e0be2c11d0df"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (71335-3021-1)", "package_ndc": "71335-3021-1", "marketing_start_date": "20251204"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-3021-2)", "package_ndc": "71335-3021-2", "marketing_start_date": "20251204"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-3021-3)", "package_ndc": "71335-3021-3", "marketing_start_date": "20251204"}], "brand_name": "Sevelamer Carbonate", "product_id": "71335-3021_5c329e0c-2108-4e78-9cfb-46a153a7319d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "71335-3021", "generic_name": "Sevelamer Carbonate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevelamer Carbonate", "active_ingredients": [{"name": "SEVELAMER CARBONATE", "strength": "800 mg/1"}], "application_number": "ANDA206100", "marketing_category": "ANDA", "marketing_start_date": "20230419", "listing_expiration_date": "20261231"}