Package 68462-447-30

Brand: sevelamer hydrochloride

Generic: sevelamer hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68462-447-30
Digits Only 6846244730
Product NDC 68462-447
Description

30 TABLET, FILM COATED in 1 BOTTLE (68462-447-30)

Marketing

Marketing Status
Marketed Since 2019-02-08
Brand sevelamer hydrochloride
Generic sevelamer hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["PARENTERAL"], "spl_id": "5b27539f-4664-4a6b-abe4-2abcc7ad2279", "openfda": {"upc": ["0368462447185", "0368462446263"], "unii": ["GLS2PGI8QG"], "rxcui": ["857216", "857224"], "spl_set_id": ["2cd6512f-0edd-4a30-a4fa-aa996038633c"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (68462-447-18)", "package_ndc": "68462-447-18", "marketing_start_date": "20190208"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68462-447-30)", "package_ndc": "68462-447-30", "marketing_start_date": "20190208"}], "brand_name": "sevelamer hydrochloride", "product_id": "68462-447_5b27539f-4664-4a6b-abe4-2abcc7ad2279", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "68462-447", "generic_name": "sevelamer hydrochloride", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "sevelamer hydrochloride", "active_ingredients": [{"name": "SEVELAMER HYDROCHLORIDE", "strength": "800 mg/1"}], "application_number": "ANDA204724", "marketing_category": "ANDA", "marketing_start_date": "20190208", "listing_expiration_date": "20271231"}