raloxifene hydrochloride

Generic: raloxifene

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name raloxifene hydrochloride
Generic Name raloxifene
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

raloxifene hydrochloride 60 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-266
Product ID 60687-266_18588c41-973d-4ebc-e063-6294a90a5eed
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090842
Listing Expiration 2026-12-31
Marketing Start 2016-11-09

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687266
Hyphenated Format 60687-266

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 (source: ndc)
Application Number ANDA090842 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-266-21) / 1 TABLET in 1 BLISTER PACK (60687-266-11)
source: ndc

Packages (1)

60687-266-21 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-266-21) / 1 TABLET in 1 BLISTER PACK (60687-266-11)

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": "18588c41-973d-4ebc-e063-6294a90a5eed", "openfda": {"unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["f5c25553-1546-451d-8069-c0f484c47741"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-266-21)  / 1 TABLET in 1 BLISTER PACK (60687-266-11)", "package_ndc": "60687-266-21", "marketing_start_date": "20161109"}], "brand_name": "Raloxifene Hydrochloride", "product_id": "60687-266_18588c41-973d-4ebc-e063-6294a90a5eed", "dosage_form": "TABLET", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "60687-266", "generic_name": "Raloxifene", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Raloxifene Hydrochloride", "active_ingredients": [{"name": "RALOXIFENE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA090842", "marketing_category": "ANDA", "marketing_start_date": "20161109", "listing_expiration_date": "20261231"}