raloxifene hydrochloride

Generic: raloxifene hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name raloxifene hydrochloride
Generic Name raloxifene hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

raloxifene hydrochloride 60 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1715
Product ID 71335-1715_8f53d830-2fb0-400c-8f03-f81858280782
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078193
Listing Expiration 2026-12-31
Marketing Start 2014-03-28

Pharmacologic Class

Classes
estrogen agonist/antagonist [epc] selective estrogen receptor modulators [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351715
Hyphenated Format 71335-1715

Supplemental Identifiers

RxCUI
1490065
UNII
4F86W47BR6

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 raloxifene hydrochloride (source: ndc)
Generic Name raloxifene hydrochloride (source: ndc)
Application Number ANDA078193 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-1715-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-1715-2)
source: ndc

Packages (2)

71335-1715-1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1715-1) 71335-1715-2 30 TABLET, FILM COATED in 1 BOTTLE (71335-1715-2)

Ingredients (1)

raloxifene hydrochloride (60 mg/1)

Linked Drug Pages (1)

Raloxifene Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8f53d830-2fb0-400c-8f03-f81858280782", "openfda": {"unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["3568ed3c-6afd-4872-a861-93a7873bec9c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1715-1)", "package_ndc": "71335-1715-1", "marketing_start_date": "20201002"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1715-2)", "package_ndc": "71335-1715-2", "marketing_start_date": "20211229"}], "brand_name": "Raloxifene Hydrochloride", "product_id": "71335-1715_8f53d830-2fb0-400c-8f03-f81858280782", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "71335-1715", "generic_name": "Raloxifene Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Raloxifene Hydrochloride", "active_ingredients": [{"name": "RALOXIFENE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA078193", "marketing_category": "ANDA", "marketing_start_date": "20140328", "listing_expiration_date": "20261231"}