Package 76282-407-27

Brand: sevelamer carbonate

Generic: sevelamer carbonate
NDC Package

Package Facts

Identity

Package NDC 76282-407-27
Digits Only 7628240727
Product NDC 76282-407
Description

270 TABLET, FILM COATED in 1 BOTTLE (76282-407-27)

Marketing

Marketing Status
Marketed Since 2017-11-08
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": "531e94a5-1e37-446c-879a-bafeedf64bd5", "openfda": {"upc": ["0376282407272"], "unii": ["9YCX42I8IU"], "rxcui": ["749206"], "spl_set_id": ["568b8558-6117-4c2f-aabf-86e567b38863"], "manufacturer_name": ["Exelan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE (76282-407-27)", "package_ndc": "76282-407-27", "marketing_start_date": "20171108"}], "brand_name": "Sevelamer carbonate", "product_id": "76282-407_531e94a5-1e37-446c-879a-bafeedf64bd5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "76282-407", "generic_name": "SEVELAMER CARBONATE", "labeler_name": "Exelan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevelamer carbonate", "active_ingredients": [{"name": "SEVELAMER CARBONATE", "strength": "800 mg/1"}], "application_number": "ANDA203860", "marketing_category": "ANDA", "marketing_start_date": "20171108", "listing_expiration_date": "20261231"}