Package 69452-158-25

Brand: colesevelam hydrochloride

Generic: colesevelam hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69452-158-25
Digits Only 6945215825
Product NDC 69452-158
Product ID 69452-158_30b35341-6379-12e6-e063-6394a90ad2c6
Description

180 TABLET, FILM COATED in 1 BOTTLE (69452-158-25)

Marketing

Marketing Status
Marketed Since 2019-12-02
Brand colesevelam hydrochloride
Generic colesevelam hydrochloride
Sample Package No

Linked Drug Pages (1)

COLESEVELAM HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "30b35341-6379-12e6-e063-6394a90ad2c6", "openfda": {"unii": ["P4SG24WI5Q"], "rxcui": ["866910"], "spl_set_id": ["a2c5e881-2901-4f90-95cc-74930569e51e"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (69452-158-25)", "package_ndc": "69452-158-25", "marketing_start_date": "20191202"}], "brand_name": "COLESEVELAM HYDROCHLORIDE", "product_id": "69452-158_30b35341-6379-12e6-e063-6394a90ad2c6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bile Acid Sequestrant [EPC]", "Bile-acid Binding Activity [MoA]"], "product_ndc": "69452-158", "generic_name": "colesevelam hydrochloride", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "COLESEVELAM HYDROCHLORIDE", "active_ingredients": [{"name": "COLESEVELAM HYDROCHLORIDE", "strength": "625 mg/1"}], "application_number": "ANDA208670", "marketing_category": "ANDA", "marketing_start_date": "20191202", "listing_expiration_date": "20261231"}