Package 0955-1050-27

Brand: sevelamer carbonate

Generic: sevelamer carbonate
NDC Package

Package Facts

Identity

Package NDC 0955-1050-27
Digits Only 0955105027
Product NDC 0955-1050
Description

270 TABLET, FILM COATED in 1 BOTTLE (0955-1050-27)

Marketing

Marketing Status
Marketed Since 2018-02-01
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": "42bdb389-5550-487c-aed2-c4e3afd239c8", "openfda": {"unii": ["9YCX42I8IU"], "rxcui": ["749206", "861370", "861375"], "spl_set_id": ["3abc32fe-1bfc-4759-8f7c-36095e221b06"], "manufacturer_name": ["Sanofi-Aventis U.S. LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE (0955-1050-27)", "package_ndc": "0955-1050-27", "marketing_start_date": "20180201"}], "brand_name": "Sevelamer Carbonate", "product_id": "0955-1050_42bdb389-5550-487c-aed2-c4e3afd239c8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "0955-1050", "generic_name": "Sevelamer Carbonate", "labeler_name": "Sanofi-Aventis U.S. LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevelamer Carbonate", "active_ingredients": [{"name": "SEVELAMER CARBONATE", "strength": "800 mg/1"}], "application_number": "NDA022127", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20180201", "listing_expiration_date": "20261231"}