colestipol hydrochloride
Generic: colestipol hydrochloride
Labeler: zydus lifesciences limitedDrug Facts
Product Profile
Brand Name
colestipol hydrochloride
Generic Name
colestipol hydrochloride
Labeler
zydus lifesciences limited
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
colestipol hydrochloride 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
70771-1653
Product ID
70771-1653_e5237070-d3ba-4dd6-921d-7ec80d8bc251
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215223
Listing Expiration
2026-12-31
Marketing Start
2022-05-04
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
707711653
Hyphenated Format
70771-1653
Supplemental Identifiers
RxCUI
UPC
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
colestipol hydrochloride (source: ndc)
Generic Name
colestipol hydrochloride (source: ndc)
Application Number
ANDA215223 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 500 TABLET, FILM COATED in 1 BOTTLE (70771-1653-5)
- 120 TABLET, FILM COATED in 1 BOTTLE (70771-1653-7)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e5237070-d3ba-4dd6-921d-7ec80d8bc251", "openfda": {"upc": ["0370771165377"], "unii": ["X7D10K905G"], "rxcui": ["1048445"], "spl_set_id": ["3b451f0b-5bd9-419a-afa2-a02eb0bbc45e"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (70771-1653-5)", "package_ndc": "70771-1653-5", "marketing_start_date": "20220504"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (70771-1653-7)", "package_ndc": "70771-1653-7", "marketing_start_date": "20220504"}], "brand_name": "Colestipol hydrochloride", "product_id": "70771-1653_e5237070-d3ba-4dd6-921d-7ec80d8bc251", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bile Acid Sequestrant [EPC]", "Bile-acid Binding Activity [MoA]"], "product_ndc": "70771-1653", "generic_name": "Colestipol hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Colestipol hydrochloride", "active_ingredients": [{"name": "COLESTIPOL HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "ANDA215223", "marketing_category": "ANDA", "marketing_start_date": "20220504", "listing_expiration_date": "20261231"}