sevelamer carbonate

Generic: sevelamer carbonate

Labeler: exelan pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sevelamer carbonate
Generic Name sevelamer carbonate
Labeler exelan pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sevelamer carbonate 800 mg/1

Manufacturer
Exelan Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 76282-407
Product ID 76282-407_531e94a5-1e37-446c-879a-bafeedf64bd5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203860
Listing Expiration 2026-12-31
Marketing Start 2017-11-08

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76282407
Hyphenated Format 76282-407

Supplemental Identifiers

RxCUI
749206
UPC
0376282407272
UNII
9YCX42I8IU

Packaging Origin

Original Packager
true

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 ANDA203860 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 800 mg/1
source: ndc
Packaging
  • 270 TABLET, FILM COATED in 1 BOTTLE (76282-407-27)
source: ndc

Packages (1)

Ingredients (1)

sevelamer carbonate (800 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "531e94a5-1e37-446c-879a-bafeedf64bd5", "openfda": {"upc": ["0376282407272"], "unii": ["9YCX42I8IU"], "rxcui": ["749206"], "spl_set_id": ["568b8558-6117-4c2f-aabf-86e567b38863"], "manufacturer_name": ["Exelan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE (76282-407-27)", "package_ndc": "76282-407-27", "marketing_start_date": "20171108"}], "brand_name": "Sevelamer carbonate", "product_id": "76282-407_531e94a5-1e37-446c-879a-bafeedf64bd5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "76282-407", "generic_name": "SEVELAMER CARBONATE", "labeler_name": "Exelan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevelamer carbonate", "active_ingredients": [{"name": "SEVELAMER CARBONATE", "strength": "800 mg/1"}], "application_number": "ANDA203860", "marketing_category": "ANDA", "marketing_start_date": "20171108", "listing_expiration_date": "20261231"}