NDC 51672-5306 – Fluoxetine Hydrochloride
Fluoxetine Hydrochloride 60 mg/1 · Tablet, Film Coated · Oral
Product NDC51672-5306
Product details
- Brand name
- Fluoxetine Hydrochloride
- Generic name
- Fluoxetine Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA211477
- Marketed since
- February 15, 2019
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Fluoxetine Hydrochloride 60 mg/1
Uses, dosage, side effects and warnings for Fluoxetine hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51672-5306-2 | 500 TABLET, FILM COATED in 1 BOTTLE (51672-5306-2) | Feb 15, 2019 |
| 51672-5306-6 | 30 TABLET, FILM COATED in 1 BOTTLE (51672-5306-6) | Feb 15, 2019 |
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