Package 0115-1320-19

Brand: colesevelam hydrochloride

Generic: colesevelam hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0115-1320-19
Digits Only 0115132019
Product NDC 0115-1320
Description

180 TABLET, FILM COATED in 1 BOTTLE (0115-1320-19)

Marketing

Marketing Status
Marketed Since 2018-05-17
Brand colesevelam hydrochloride
Generic colesevelam hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6fbde16a-69db-42e0-9e63-86c1116ae99f", "openfda": {"upc": ["0301151320192"], "unii": ["P4SG24WI5Q"], "rxcui": ["866910"], "spl_set_id": ["f5306376-e7f2-44ad-8250-635b95428a7c"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (0115-1320-19)", "package_ndc": "0115-1320-19", "marketing_start_date": "20180517"}], "brand_name": "Colesevelam Hydrochloride", "product_id": "0115-1320_6fbde16a-69db-42e0-9e63-86c1116ae99f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bile Acid Sequestrant [EPC]", "Bile-acid Binding Activity [MoA]"], "product_ndc": "0115-1320", "generic_name": "COLESEVELAM HYDROCHLORIDE", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Colesevelam Hydrochloride", "active_ingredients": [{"name": "COLESEVELAM HYDROCHLORIDE", "strength": "625 mg/1"}], "application_number": "ANDA091600", "marketing_category": "ANDA", "marketing_start_date": "20180517", "listing_expiration_date": "20261231"}