Package 70710-1467-5

Brand: colestipol hydrochloride

Generic: colestipol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70710-1467-5
Digits Only 7071014675
Product NDC 70710-1467
Description

500 TABLET, FILM COATED in 1 BOTTLE (70710-1467-5)

Marketing

Marketing Status
Marketed Since 2022-05-04
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": "f8cd3220-beeb-49b7-845a-d1bbb0476377", "openfda": {"upc": ["0370710146771"], "unii": ["X7D10K905G"], "rxcui": ["1048445"], "spl_set_id": ["71f12e0d-373a-4867-b37c-f24d99c5ce95"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (70710-1467-5)", "package_ndc": "70710-1467-5", "marketing_start_date": "20220504"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (70710-1467-7)", "package_ndc": "70710-1467-7", "marketing_start_date": "20220504"}], "brand_name": "Colestipol hydrochloride", "product_id": "70710-1467_f8cd3220-beeb-49b7-845a-d1bbb0476377", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bile Acid Sequestrant [EPC]", "Bile-acid Binding Activity [MoA]"], "product_ndc": "70710-1467", "generic_name": "Colestipol hydrochloride", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Colestipol hydrochloride", "active_ingredients": [{"name": "COLESTIPOL HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "ANDA215223", "marketing_category": "ANDA", "marketing_start_date": "20220504", "listing_expiration_date": "20261231"}