Package 60687-715-21

Brand: colestipol hydrochloride

Generic: colestipol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-715-21
Digits Only 6068771521
Product NDC 60687-715
Description

30 BLISTER PACK in 1 CARTON (60687-715-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-715-11)

Marketing

Marketing Status
Marketed Since 2023-05-10
Brand colestipol hydrochloride
Generic colestipol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "401f73b1-98f5-b6d1-e063-6394a90acf6e", "openfda": {"unii": ["X7D10K905G"], "rxcui": ["1048445"], "spl_set_id": ["153e9154-1804-4d73-94b7-a31a1d37c420"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-715-21)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-715-11)", "package_ndc": "60687-715-21", "marketing_start_date": "20230510"}], "brand_name": "Colestipol Hydrochloride", "product_id": "60687-715_401f73b1-98f5-b6d1-e063-6394a90acf6e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bile Acid Sequestrant [EPC]", "Bile-acid Binding Activity [MoA]"], "product_ndc": "60687-715", "generic_name": "Colestipol Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Colestipol Hydrochloride", "active_ingredients": [{"name": "COLESTIPOL HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "ANDA077510", "marketing_category": "ANDA", "marketing_start_date": "20230510", "listing_expiration_date": "20261231"}