sevelamer carbonate
Generic: sevelamer carbonate
Labeler: exelan pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
sevelamer carbonate
Generic Name
sevelamer carbonate
Labeler
exelan pharmaceuticals inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
sevelamer carbonate 800 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76282407
Hyphenated Format
76282-407
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 800 mg/1
Packaging
- 270 TABLET, FILM COATED in 1 BOTTLE (76282-407-27)
Packages (1)
Ingredients (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"}