Package 50742-284-12

Brand: colestipol hydrochloride

Generic: colestipol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50742-284-12
Digits Only 5074228412
Product NDC 50742-284
Description

120 TABLET, FILM COATED in 1 BOTTLE (50742-284-12)

Marketing

Marketing Status
Marketed Since 2024-12-03
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": "f784d09d-69b6-4e7b-a1eb-8b7e839cd4db", "openfda": {"upc": ["0350742284122"], "unii": ["X7D10K905G"], "rxcui": ["1048445"], "spl_set_id": ["3fa27483-8346-4145-81c0-5527204d7d68"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (50742-284-12)", "package_ndc": "50742-284-12", "marketing_start_date": "20241203"}], "brand_name": "Colestipol Hydrochloride", "product_id": "50742-284_f784d09d-69b6-4e7b-a1eb-8b7e839cd4db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bile Acid Sequestrant [EPC]", "Bile-acid Binding Activity [MoA]"], "product_ndc": "50742-284", "generic_name": "Colestipol Hydrochloride", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Colestipol Hydrochloride", "active_ingredients": [{"name": "COLESTIPOL HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "ANDA217462", "marketing_category": "ANDA", "marketing_start_date": "20241203", "listing_expiration_date": "20261231"}