Package 58468-0133-1

Brand: renvela

Generic: sevelamer carbonate
NDC Package

Package Facts

Identity

Package NDC 58468-0133-1
Digits Only 5846801331
Product NDC 58468-0133
Description

270 TABLET, FILM COATED in 1 BOTTLE (58468-0133-1)

Marketing

Marketing Status
Marketed Since 2023-07-14
Brand renvela
Generic sevelamer carbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cb4453a2-c47b-4352-839f-f022ac67368e", "openfda": {"unii": ["9YCX42I8IU"], "rxcui": ["749206", "749210", "861370", "861373", "861375", "861377"], "spl_set_id": ["e6328460-a57b-450b-a48c-6dcd4b476360"], "manufacturer_name": ["Genzyme Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE (58468-0133-1)", "package_ndc": "58468-0133-1", "marketing_start_date": "20230714"}], "brand_name": "Renvela", "product_id": "58468-0133_cb4453a2-c47b-4352-839f-f022ac67368e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "58468-0133", "generic_name": "SEVELAMER CARBONATE", "labeler_name": "Genzyme Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Renvela", "active_ingredients": [{"name": "SEVELAMER CARBONATE", "strength": "800 mg/1"}], "application_number": "NDA022127", "marketing_category": "NDA", "marketing_start_date": "20090812", "listing_expiration_date": "20261231"}