colesevelam hydrochloride
Generic: colesevelam hydrochloride
Labeler: bionpharma inc.Drug Facts
Product Profile
Brand Name
colesevelam hydrochloride
Generic Name
colesevelam hydrochloride
Labeler
bionpharma inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
colesevelam hydrochloride 625 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69452-158
Product ID
69452-158_30b35341-6379-12e6-e063-6394a90ad2c6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208670
Listing Expiration
2026-12-31
Marketing Start
2019-12-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69452158
Hyphenated Format
69452-158
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
colesevelam hydrochloride (source: ndc)
Generic Name
colesevelam hydrochloride (source: ndc)
Application Number
ANDA208670 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 625 mg/1
Packaging
- 180 TABLET, FILM COATED in 1 BOTTLE (69452-158-25)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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"}