Package 42799-115-01

Brand: colestipol hydrochloride

Generic: colestipol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42799-115-01
Digits Only 4279911501
Product NDC 42799-115
Product ID 42799-115_440d1d49-3eb7-42db-8536-9f0a91c46532
Description

120 TABLET in 1 BOTTLE (42799-115-01)

Marketing

Marketing Status
Marketed Since 2024-11-26
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": "440d1d49-3eb7-42db-8536-9f0a91c46532", "openfda": {"upc": ["0342799115016"], "unii": ["X7D10K905G"], "rxcui": ["1048445"], "spl_set_id": ["03ca5800-4211-4383-a332-be88bd9b5304"], "manufacturer_name": ["Edenbridge Pharmaceuticals LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (42799-115-01)", "package_ndc": "42799-115-01", "marketing_start_date": "20241126"}], "brand_name": "Colestipol Hydrochloride", "product_id": "42799-115_440d1d49-3eb7-42db-8536-9f0a91c46532", "dosage_form": "TABLET", "pharm_class": ["Bile Acid Sequestrant [EPC]", "Bile-acid Binding Activity [MoA]"], "product_ndc": "42799-115", "generic_name": "Colestipol Hydrochloride", "labeler_name": "Edenbridge Pharmaceuticals LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Colestipol Hydrochloride", "active_ingredients": [{"name": "COLESTIPOL HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "ANDA217667", "marketing_category": "ANDA", "marketing_start_date": "20241126", "listing_expiration_date": "20261231"}