Package 62559-395-12
Brand: colestipol hydrochloride
Generic: colestipol hydrochloridePackage Facts
Identity
Package NDC
62559-395-12
Digits Only
6255939512
Product NDC
62559-395
Description
120 TABLET, FILM COATED in 1 BOTTLE (62559-395-12)
Marketing
Marketing Status
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": "f062e9d4-c5ef-411e-8f4a-6deec3ee95c7", "openfda": {"upc": ["0362559395120"], "unii": ["X7D10K905G"], "rxcui": ["1048445"], "spl_set_id": ["3d380b5e-e346-4a47-ac95-faa37c6f2a51"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (62559-395-12)", "package_ndc": "62559-395-12", "marketing_start_date": "20230515"}], "brand_name": "COLESTIPOL HYDROCHLORIDE", "product_id": "62559-395_f062e9d4-c5ef-411e-8f4a-6deec3ee95c7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bile Acid Sequestrant [EPC]", "Bile-acid Binding Activity [MoA]"], "product_ndc": "62559-395", "generic_name": "COLESTIPOL HYDROCHLORIDE", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "COLESTIPOL HYDROCHLORIDE", "active_ingredients": [{"name": "COLESTIPOL HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "ANDA216517", "marketing_category": "ANDA", "marketing_start_date": "20230515", "listing_expiration_date": "20261231"}