sevelamer carbonate
Generic: sevelamer carbonate
Labeler: twi pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
sevelamer carbonate
Generic Name
sevelamer carbonate
Labeler
twi pharmaceuticals, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
sevelamer carbonate 800 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
24979-186
Product ID
24979-186_ddf1d2bb-b32a-4fb1-9e0e-1b3047c9b448
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA200959
Marketing Start
2019-09-30
Marketing End
2026-11-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
24979186
Hyphenated Format
24979-186
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
ANDA200959 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 800 mg/1
Packaging
- 270 TABLET, FILM COATED in 1 BOTTLE (24979-186-46)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ddf1d2bb-b32a-4fb1-9e0e-1b3047c9b448", "openfda": {"upc": ["0324979186467"], "unii": ["9YCX42I8IU"], "rxcui": ["749206"], "spl_set_id": ["05b076d9-6516-4538-8e05-9709a677ed2f"], "manufacturer_name": ["TWi Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE (24979-186-46)", "package_ndc": "24979-186-46", "marketing_end_date": "20261130", "marketing_start_date": "20190930"}], "brand_name": "Sevelamer Carbonate", "product_id": "24979-186_ddf1d2bb-b32a-4fb1-9e0e-1b3047c9b448", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "24979-186", "generic_name": "Sevelamer Carbonate", "labeler_name": "TWi Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevelamer Carbonate", "active_ingredients": [{"name": "SEVELAMER CARBONATE", "strength": "800 mg/1"}], "application_number": "ANDA200959", "marketing_category": "ANDA", "marketing_end_date": "20261130", "marketing_start_date": "20190930"}