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, COATED
Routes
ORAL
Active Ingredients

raloxifene hydrochloride 60 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2418
Product ID 72162-2418_098f2903-afc3-4a47-8c22-9cc1ce9d50c3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211324
Listing Expiration 2026-12-31
Marketing Start 2017-12-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622418
Hyphenated Format 72162-2418

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 ANDA211324 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
source: ndc
Packaging
  • 1000 TABLET, COATED in 1 BOTTLE (72162-2418-0)
  • 100 TABLET, COATED in 1 BOTTLE (72162-2418-1)
  • 30 TABLET, COATED in 1 BOTTLE (72162-2418-3)
source: ndc

Packages (3)

72162-2418-0 1000 TABLET, COATED in 1 BOTTLE (72162-2418-0) 72162-2418-1 100 TABLET, COATED in 1 BOTTLE (72162-2418-1) 72162-2418-3 30 TABLET, COATED in 1 BOTTLE (72162-2418-3)

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": "098f2903-afc3-4a47-8c22-9cc1ce9d50c3", "openfda": {"unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["7e4bfee5-fefc-4115-9bdb-222eccefca83"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (72162-2418-0)", "package_ndc": "72162-2418-0", "marketing_start_date": "20241031"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (72162-2418-1)", "package_ndc": "72162-2418-1", "marketing_start_date": "20241031"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (72162-2418-3)", "package_ndc": "72162-2418-3", "marketing_start_date": "20241031"}], "brand_name": "Raloxifene hydrochloride", "product_id": "72162-2418_098f2903-afc3-4a47-8c22-9cc1ce9d50c3", "dosage_form": "TABLET, COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "72162-2418", "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": "ANDA211324", "marketing_category": "ANDA", "marketing_start_date": "20171230", "listing_expiration_date": "20261231"}