raloxifene hydrochloride

Generic: raloxifene hydrochloride

Labeler: dr.reddys laboratories inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name raloxifene hydrochloride
Generic Name raloxifene hydrochloride
Labeler dr.reddys laboratories inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

raloxifene hydrochloride 60 mg/1

Manufacturer
Dr.Reddys Laboratories Inc

Identifiers & Regulatory

Product NDC 43598-505
Product ID 43598-505_f08636b3-11f2-23f1-e053-2a95a90a12e5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206384
Listing Expiration 2026-12-31
Marketing Start 2016-10-12

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43598505
Hyphenated Format 43598-505

Supplemental Identifiers

RxCUI
1490065
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 ANDA206384 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (43598-505-01)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (43598-505-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (43598-505-30)
source: ndc

Packages (3)

43598-505-01 100 TABLET, FILM COATED in 1 BOTTLE (43598-505-01) 43598-505-10 1000 TABLET, FILM COATED in 1 BOTTLE (43598-505-10) 43598-505-30 30 TABLET, FILM COATED in 1 BOTTLE (43598-505-30)

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": "f08636b3-11f2-23f1-e053-2a95a90a12e5", "openfda": {"unii": ["4F86W47BR6"], "rxcui": ["1490065"], "spl_set_id": ["8f24455c-34dc-4e07-bcd3-24326b9cc377"], "manufacturer_name": ["Dr.Reddys Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (43598-505-01)", "package_ndc": "43598-505-01", "marketing_start_date": "20161012"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (43598-505-10)", "package_ndc": "43598-505-10", "marketing_start_date": "20161012"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (43598-505-30)", "package_ndc": "43598-505-30", "marketing_start_date": "20161012"}], "brand_name": "Raloxifene hydrochloride", "product_id": "43598-505_f08636b3-11f2-23f1-e053-2a95a90a12e5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "43598-505", "generic_name": "Raloxifene hydrochloride", "labeler_name": "Dr.Reddys Laboratories Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Raloxifene hydrochloride", "active_ingredients": [{"name": "RALOXIFENE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA206384", "marketing_category": "ANDA", "marketing_start_date": "20161012", "listing_expiration_date": "20261231"}