Package 69367-423-27

Brand: sevelamer carbonate

Generic: sevelamer carbonate
NDC Package

Package Facts

Identity

Package NDC 69367-423-27
Digits Only 6936742327
Product NDC 69367-423
Product ID 69367-423_f63f474a-c262-4d88-bb90-a25425bdd296
Description

270 TABLET, FILM COATED in 1 BOTTLE (69367-423-27)

Marketing

Marketing Status
Marketed Since 2025-09-23
Brand sevelamer carbonate
Generic sevelamer carbonate
Sample Package No

Linked Drug Pages (1)

Sevelamer Carbonate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f63f474a-c262-4d88-bb90-a25425bdd296", "openfda": {"upc": ["0369367423274"], "unii": ["9YCX42I8IU"], "rxcui": ["749206"], "spl_set_id": ["45a955e9-94ac-48db-838c-74934eae245b"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE (69367-423-27)", "package_ndc": "69367-423-27", "marketing_start_date": "20250923"}], "brand_name": "Sevelamer Carbonate", "product_id": "69367-423_f63f474a-c262-4d88-bb90-a25425bdd296", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "69367-423", "generic_name": "Sevelamer Carbonate", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevelamer Carbonate", "active_ingredients": [{"name": "SEVELAMER CARBONATE", "strength": "800 mg/1"}], "application_number": "ANDA200959", "marketing_category": "ANDA", "marketing_start_date": "20250923", "listing_expiration_date": "20261231"}