colestipol hydrochloride

Generic: colestipol hydrochloride

Labeler: zydus pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name colestipol hydrochloride
Generic Name colestipol hydrochloride
Labeler zydus pharmaceuticals usa inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

colestipol hydrochloride 1 g/1

Manufacturer
Zydus Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 70710-1467
Product ID 70710-1467_f8cd3220-beeb-49b7-845a-d1bbb0476377
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215223
Listing Expiration 2026-12-31
Marketing Start 2022-05-04

Pharmacologic Class

Classes
bile acid sequestrant [epc] bile-acid binding activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707101467
Hyphenated Format 70710-1467

Supplemental Identifiers

RxCUI
1048445
UPC
0370710146771
UNII
X7D10K905G

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (70710-1467-5)
  • 120 TABLET, FILM COATED in 1 BOTTLE (70710-1467-7)
source: ndc

Packages (2)

70710-1467-5 500 TABLET, FILM COATED in 1 BOTTLE (70710-1467-5) 70710-1467-7 120 TABLET, FILM COATED in 1 BOTTLE (70710-1467-7)

Ingredients (1)

colestipol hydrochloride (1 g/1)

Linked Drug Pages (1)

Colestipol hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f8cd3220-beeb-49b7-845a-d1bbb0476377", "openfda": {"upc": ["0370710146771"], "unii": ["X7D10K905G"], "rxcui": ["1048445"], "spl_set_id": ["71f12e0d-373a-4867-b37c-f24d99c5ce95"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (70710-1467-5)", "package_ndc": "70710-1467-5", "marketing_start_date": "20220504"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (70710-1467-7)", "package_ndc": "70710-1467-7", "marketing_start_date": "20220504"}], "brand_name": "Colestipol hydrochloride", "product_id": "70710-1467_f8cd3220-beeb-49b7-845a-d1bbb0476377", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bile Acid Sequestrant [EPC]", "Bile-acid Binding Activity [MoA]"], "product_ndc": "70710-1467", "generic_name": "Colestipol hydrochloride", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "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"}