Package 72162-2501-2

Brand: sevelamer hydrochloride

Generic: sevelamer hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2501-2
Digits Only 7216225012
Product NDC 72162-2501
Product ID 72162-2501_3533c2ca-1653-8676-e063-6294a90a6a59
Description

180 TABLET, FILM COATED in 1 BOTTLE (72162-2501-2)

Marketing

Marketing Status
Marketed Since 2025-05-15
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": "3533c2ca-1653-8676-e063-6294a90a6a59", "openfda": {"unii": ["GLS2PGI8QG"], "rxcui": ["857224"], "spl_set_id": ["3533d24b-508e-f012-e063-6394a90acaf5"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (72162-2501-2)", "package_ndc": "72162-2501-2", "marketing_start_date": "20250515"}], "brand_name": "Sevelamer Hydrochloride", "product_id": "72162-2501_3533c2ca-1653-8676-e063-6294a90a6a59", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "72162-2501", "generic_name": "Sevelamer Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevelamer Hydrochloride", "active_ingredients": [{"name": "SEVELAMER HYDROCHLORIDE", "strength": "800 mg/1"}], "application_number": "ANDA206883", "marketing_category": "ANDA", "marketing_start_date": "20230526", "listing_expiration_date": "20261231"}