United States · FDA National Drug Code directory
Raloxifene Hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 69097-825_ebab2c47-9350-447a-9372-7ade623d5bb1
- Product NDC
- 69097-825
- Form
- TABLET
- Composition / generic term
- Raloxifene
- Labeler
- Cipla USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160629
- Source listing expiry
- 20261231
Source-listed ingredients
- RALOXIFENE HYDROCHLORIDE — 60 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (69097-825-02) · 69097-825-02
- 100 TABLET in 1 BOTTLE (69097-825-07) · 69097-825-07
- 1000 TABLET in 1 BOTTLE (69097-825-15) · 69097-825-15
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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