colestipol hydrochloride
Generic: colestipol hydrochloride
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
colestipol hydrochloride
Generic Name
colestipol hydrochloride
Labeler
american health packaging
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
colestipol hydrochloride 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
60687-715
Product ID
60687-715_401f73b1-98f5-b6d1-e063-6394a90acf6e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077510
Listing Expiration
2026-12-31
Marketing Start
2023-05-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687715
Hyphenated Format
60687-715
Supplemental Identifiers
RxCUI
UNII
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
colestipol hydrochloride (source: ndc)
Generic Name
colestipol hydrochloride (source: ndc)
Application Number
ANDA077510 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 30 BLISTER PACK in 1 CARTON (60687-715-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-715-11)
Packages (1)
Ingredients (1)
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"}