raloxifene hydrochloride

Generic: raloxifene hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name raloxifene hydrochloride
Generic Name raloxifene hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

raloxifene hydrochloride 60 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6177
Product ID 50090-6177_88a25d54-f913-4a43-9f04-9ab1979ff633
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 500906177
Hyphenated Format 50090-6177

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
  • 90 TABLET, COATED in 1 BOTTLE (50090-6177-1)
source: ndc

Packages (1)

50090-6177-1 90 TABLET, COATED in 1 BOTTLE (50090-6177-1)

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": "88a25d54-f913-4a43-9f04-9ab1979ff633", "openfda": {"unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["22a951ee-2ffc-4c60-b681-0f80285153e1"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (50090-6177-1)", "package_ndc": "50090-6177-1", "marketing_start_date": "20221018"}], "brand_name": "Raloxifene hydrochloride", "product_id": "50090-6177_88a25d54-f913-4a43-9f04-9ab1979ff633", "dosage_form": "TABLET, COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "50090-6177", "generic_name": "Raloxifene hydrochloride", "labeler_name": "A-S Medication Solutions", "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"}