Package 59762-0450-1

Brand: colestipol hydrochloride

Generic: colestipol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59762-0450-1
Digits Only 5976204501
Product NDC 59762-0450
Product ID 59762-0450_1b610c4a-a8dc-4a10-bd7a-3e94ca49ee9c
Description

120 TABLET in 1 BOTTLE (59762-0450-1)

Marketing

Marketing Status
Marketed Since 1994-07-19
Brand colestipol hydrochloride
Generic colestipol hydrochloride
Sample Package No

Linked Drug Pages (1)

Colestipol Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1b610c4a-a8dc-4a10-bd7a-3e94ca49ee9c", "openfda": {"unii": ["X7D10K905G"], "rxcui": ["1048445"], "spl_set_id": ["dae7d51e-c117-4c8a-b018-45b01ae46100"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (59762-0450-1)", "package_ndc": "59762-0450-1", "marketing_start_date": "19940719"}], "brand_name": "Colestipol Hydrochloride", "product_id": "59762-0450_1b610c4a-a8dc-4a10-bd7a-3e94ca49ee9c", "dosage_form": "TABLET", "pharm_class": ["Bile Acid Sequestrant [EPC]", "Bile-acid Binding Activity [MoA]"], "product_ndc": "59762-0450", "generic_name": "Colestipol Hydrochloride", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Colestipol Hydrochloride", "active_ingredients": [{"name": "COLESTIPOL HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "NDA020222", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "19940719", "listing_expiration_date": "20261231"}