Package 0955-1048-18
Brand: sevelamer hydrochloride
Generic: sevelamer hydrochloridePackage Facts
Identity
Package NDC
0955-1048-18
Digits Only
0955104818
Product NDC
0955-1048
Description
180 TABLET, FILM COATED in 1 BOTTLE (0955-1048-18)
Marketing
Marketing Status
Brand
sevelamer hydrochloride
Generic
sevelamer hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c080f078-1f48-42cb-9e3c-74ed2d395e1f", "openfda": {"unii": ["GLS2PGI8QG"], "rxcui": ["857224"], "spl_set_id": ["5a76bd76-a6cc-46f1-bb58-660566eaec06"], "manufacturer_name": ["Sanofi-Aventis U.S. LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (0955-1048-18)", "package_ndc": "0955-1048-18", "marketing_end_date": "20260430", "marketing_start_date": "20190213"}], "brand_name": "Sevelamer Hydrochloride", "product_id": "0955-1048_c080f078-1f48-42cb-9e3c-74ed2d395e1f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "0955-1048", "generic_name": "Sevelamer Hydrochloride", "labeler_name": "Sanofi-Aventis U.S. LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevelamer Hydrochloride", "active_ingredients": [{"name": "SEVELAMER HYDROCHLORIDE", "strength": "800 mg/1"}], "application_number": "NDA021179", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260430", "marketing_start_date": "20190213"}