Package 27808-190-01
Brand: colesevelam hydrochloride
Generic: colesevelam hydrochloridePackage Facts
Identity
Package NDC
27808-190-01
Digits Only
2780819001
Product NDC
27808-190
Description
180 TABLET in 1 BOTTLE (27808-190-01)
Marketing
Marketing Status
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": "47df1b20-2cfd-483e-94cc-232339869d17", "openfda": {"upc": ["0327808190017"], "unii": ["P4SG24WI5Q"], "rxcui": ["866910"], "spl_set_id": ["5e50cc0c-03bc-444b-9d15-ea112bc0f91c"], "manufacturer_name": ["Cranbury Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET in 1 BOTTLE (27808-190-01)", "package_ndc": "27808-190-01", "marketing_start_date": "20201019"}], "brand_name": "Colesevelam hydrochloride", "product_id": "27808-190_47df1b20-2cfd-483e-94cc-232339869d17", "dosage_form": "TABLET", "pharm_class": ["Bile Acid Sequestrant [EPC]", "Bile-acid Binding Activity [MoA]"], "product_ndc": "27808-190", "generic_name": "Colesevelam hydrochloride", "labeler_name": "Cranbury Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Colesevelam hydrochloride", "active_ingredients": [{"name": "COLESEVELAM HYDROCHLORIDE", "strength": "625 mg/1"}], "application_number": "ANDA209946", "marketing_category": "ANDA", "marketing_start_date": "20201019", "listing_expiration_date": "20261231"}