Package 0115-5211-02

Brand: colestipol hydrochloride

Generic: colestipol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0115-5211-02
Digits Only 0115521102
Product NDC 0115-5211
Description

500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0115-5211-02)

Marketing

Marketing Status
Marketed Since 2021-08-17
Brand colestipol hydrochloride
Generic colestipol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ec79132-daa8-4439-bbd2-6f8c8c020e4f", "openfda": {"upc": ["0301155211168"], "unii": ["X7D10K905G"], "rxcui": ["1048445"], "spl_set_id": ["fa6c3e11-84e9-433d-aa74-7cd34336bbed"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0115-5211-02)", "package_ndc": "0115-5211-02", "marketing_start_date": "20210817"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0115-5211-16)", "package_ndc": "0115-5211-16", "marketing_start_date": "20210817"}], "brand_name": "COLESTIPOL HYDROCHLORIDE", "product_id": "0115-5211_4ec79132-daa8-4439-bbd2-6f8c8c020e4f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bile Acid Sequestrant [EPC]", "Bile-acid Binding Activity [MoA]"], "product_ndc": "0115-5211", "generic_name": "COLESTIPOL HYDROCHLORIDE", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "COLESTIPOL HYDROCHLORIDE", "active_ingredients": [{"name": "COLESTIPOL HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "ANDA077510", "marketing_category": "ANDA", "marketing_start_date": "20210817", "listing_expiration_date": "20261231"}