NDC 68462-393 – raloxifene hydrochloride
Raloxifene Hydrochloride 60 mg/1 · Tablet, Film Coated · Oral
Product NDC68462-393
Product details
- Brand name
- raloxifene hydrochloride
- Generic name
- raloxifene hydrochloride
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204491
- Marketed since
- March 22, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Estrogen Agonist/Antagonist
Active ingredients
- Raloxifene Hydrochloride 60 mg/1
Uses, dosage, side effects and warnings for Raloxifene Hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68462-393-01 | 100 TABLET, FILM COATED in 1 BOTTLE (68462-393-01) | Mar 22, 2016 |
| 68462-393-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (68462-393-10) | Mar 22, 2016 |
| 68462-393-23 | 2000 TABLET, FILM COATED in 1 BOTTLE (68462-393-23) | Mar 22, 2016 |
| 68462-393-30 | 30 TABLET, FILM COATED in 1 BOTTLE (68462-393-30) | Mar 22, 2016 |
| 68462-393-90 | 90 TABLET, FILM COATED in 1 BOTTLE (68462-393-90) | Mar 22, 2016 |
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