Package 70710-2058-8

Brand: sevelamer hydrochloride

Generic: sevelamer hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70710-2058-8
Digits Only 7071020588
Product NDC 70710-2058
Product ID 70710-2058_f9b9e637-d236-4bc0-afca-bbbf1b1747ab
Description

180 TABLET, FILM COATED in 1 BOTTLE (70710-2058-8)

Marketing

Marketing Status
Marketed Since 2025-03-01
Brand sevelamer hydrochloride
Generic sevelamer hydrochloride
Sample Package No

Linked Drug Pages (1)

Sevelamer Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f9b9e637-d236-4bc0-afca-bbbf1b1747ab", "openfda": {"unii": ["GLS2PGI8QG"], "rxcui": ["857224"], "spl_set_id": ["ddecb552-5882-4e44-8fa7-37c9234dd1b9"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (70710-2058-8)", "package_ndc": "70710-2058-8", "marketing_start_date": "20250301"}], "brand_name": "Sevelamer Hydrochloride", "product_id": "70710-2058_f9b9e637-d236-4bc0-afca-bbbf1b1747ab", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "70710-2058", "generic_name": "Sevelamer Hydrochloride", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevelamer Hydrochloride", "active_ingredients": [{"name": "SEVELAMER HYDROCHLORIDE", "strength": "800 mg/1"}], "application_number": "ANDA218966", "marketing_category": "ANDA", "marketing_start_date": "20250301", "listing_expiration_date": "20261231"}