raloxifene hydrochloride

Generic: raloxifene hydrochloride

Labeler: modavar pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name raloxifene hydrochloride
Generic Name raloxifene hydrochloride
Labeler modavar pharmaceuticals llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

raloxifene hydrochloride 60 mg/1

Manufacturer
Modavar Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72241-010
Product ID 72241-010_f0db29f5-28da-4165-94f8-24727b6b71e5
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 72241010
Hyphenated Format 72241-010

Supplemental Identifiers

RxCUI
1490065
UPC
0372241010057 0372241010224
UNII
4F86W47BR6

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 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
  • 100 TABLET, COATED in 1 BOTTLE (72241-010-05)
  • 1000 TABLET, COATED in 1 BOTTLE (72241-010-11)
  • 2000 TABLET, COATED in 1 BOTTLE (72241-010-13)
  • 30 TABLET, COATED in 1 BOTTLE (72241-010-22)
source: ndc

Packages (4)

72241-010-05 100 TABLET, COATED in 1 BOTTLE (72241-010-05) 72241-010-11 1000 TABLET, COATED in 1 BOTTLE (72241-010-11) 72241-010-13 2000 TABLET, COATED in 1 BOTTLE (72241-010-13) 72241-010-22 30 TABLET, COATED in 1 BOTTLE (72241-010-22)

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": "f0db29f5-28da-4165-94f8-24727b6b71e5", "openfda": {"upc": ["0372241010057", "0372241010224"], "unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["f0db29f5-28da-4165-94f8-24727b6b71e5"], "manufacturer_name": ["Modavar Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (72241-010-05)", "package_ndc": "72241-010-05", "marketing_start_date": "20171230"}, {"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (72241-010-11)", "package_ndc": "72241-010-11", "marketing_start_date": "20171230"}, {"sample": false, "description": "2000 TABLET, COATED in 1 BOTTLE (72241-010-13)", "package_ndc": "72241-010-13", "marketing_start_date": "20171230"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (72241-010-22)", "package_ndc": "72241-010-22", "marketing_start_date": "20171230"}], "brand_name": "Raloxifene hydrochloride", "product_id": "72241-010_f0db29f5-28da-4165-94f8-24727b6b71e5", "dosage_form": "TABLET, COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "72241-010", "generic_name": "Raloxifene hydrochloride", "labeler_name": "Modavar Pharmaceuticals LLC", "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"}