Package 72603-148-01

Brand: sevelamer hydrochloride

Generic: sevelamer hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72603-148-01
Digits Only 7260314801
Product NDC 72603-148
Product ID 72603-148_a229a42a-4d1b-45df-aa77-71f44e0921ee
Description

180 TABLET, FILM COATED in 1 BOTTLE (72603-148-01)

Marketing

Marketing Status
Marketed Since 2023-05-23
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": "a229a42a-4d1b-45df-aa77-71f44e0921ee", "openfda": {"upc": ["0372603148015"], "unii": ["GLS2PGI8QG"], "rxcui": ["857224"], "spl_set_id": ["a229a42a-4d1b-45df-aa77-71f44e0921ee"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (72603-148-01)", "package_ndc": "72603-148-01", "marketing_start_date": "20230523"}], "brand_name": "sevelamer hydrochloride", "product_id": "72603-148_a229a42a-4d1b-45df-aa77-71f44e0921ee", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "72603-148", "generic_name": "sevelamer hydrochloride", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "sevelamer hydrochloride", "active_ingredients": [{"name": "SEVELAMER HYDROCHLORIDE", "strength": "800 mg/1"}], "application_number": "ANDA204724", "marketing_category": "ANDA", "marketing_start_date": "20230523", "listing_expiration_date": "20261231"}