Package 24979-186-46
Brand: sevelamer carbonate
Generic: sevelamer carbonatePackage Facts
Identity
Package NDC
24979-186-46
Digits Only
2497918646
Product NDC
24979-186
Description
270 TABLET, FILM COATED in 1 BOTTLE (24979-186-46)
Marketing
Marketing Status
Brand
sevelamer carbonate
Generic
sevelamer carbonate
Sample Package
No
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"}