Package 59651-087-36

Brand: sevelamer hydrochloride

Generic: sevelamer hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59651-087-36
Digits Only 5965108736
Product NDC 59651-087
Product ID 59651-087_7a6f6abf-8a91-423e-8f2f-de1b3a019e7b
Description

360 TABLET, FILM COATED in 1 BOTTLE (59651-087-36)

Marketing

Marketing Status
Marketed Since 2023-07-11
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": "7a6f6abf-8a91-423e-8f2f-de1b3a019e7b", "openfda": {"unii": ["GLS2PGI8QG"], "rxcui": ["857216", "857224"], "spl_set_id": ["d8729e42-dbbd-4954-9ce0-298743a15a06"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "360 TABLET, FILM COATED in 1 BOTTLE (59651-087-36)", "package_ndc": "59651-087-36", "marketing_start_date": "20230711"}], "brand_name": "SEVELAMER HYDROCHLORIDE", "product_id": "59651-087_7a6f6abf-8a91-423e-8f2f-de1b3a019e7b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "59651-087", "generic_name": "SEVELAMER HYDROCHLORIDE", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SEVELAMER HYDROCHLORIDE", "active_ingredients": [{"name": "SEVELAMER HYDROCHLORIDE", "strength": "400 mg/1"}], "application_number": "ANDA212599", "marketing_category": "ANDA", "marketing_start_date": "20230711", "listing_expiration_date": "20261231"}