Package 0009-0450-03

Brand: colestid

Generic: colestipol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0009-0450-03
Digits Only 0009045003
Product NDC 0009-0450
Product ID 0009-0450_62a88ff5-632d-4fe7-a4e5-1170f1c70dd3
Description

120 TABLET in 1 BOTTLE (0009-0450-03)

Marketing

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

Linked Drug Pages (1)

Colestid ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "62a88ff5-632d-4fe7-a4e5-1170f1c70dd3", "openfda": {"upc": ["0300090450038"], "unii": ["X7D10K905G"], "rxcui": ["1048445", "1048447"], "spl_set_id": ["3e270911-f27b-44d4-b0a2-33506418cc1d"], "manufacturer_name": ["Pharmacia & Upjohn Company LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (0009-0450-03)", "package_ndc": "0009-0450-03", "marketing_start_date": "19940719"}], "brand_name": "Colestid", "product_id": "0009-0450_62a88ff5-632d-4fe7-a4e5-1170f1c70dd3", "dosage_form": "TABLET", "pharm_class": ["Bile Acid Sequestrant [EPC]", "Bile-acid Binding Activity [MoA]"], "product_ndc": "0009-0450", "generic_name": "Colestipol Hydrochloride", "labeler_name": "Pharmacia & Upjohn Company LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Colestid", "active_ingredients": [{"name": "COLESTIPOL HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "NDA020222", "marketing_category": "NDA", "marketing_start_date": "19940719", "listing_expiration_date": "20261231"}