NDC 43598-632 – Fluoxetine hydrochloride
Fluoxetine Hydrochloride 60 mg/1 · Tablet, Film Coated · Oral
Product NDC43598-632
Product details
- Brand name
- Fluoxetine hydrochloride
- Generic name
- Fluoxetine hydrochloride
- Labeler
- Dr. Reddy's Laboratories Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA211721
- Marketed since
- January 28, 2019
- Listing expires
- December 31, 2026
- 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 |
|---|---|---|
| 43598-632-01 | 100 TABLET, FILM COATED in 1 BOTTLE (43598-632-01) | Jan 28, 2019 |
| 43598-632-30 | 30 TABLET, FILM COATED in 1 BOTTLE (43598-632-30) | Jan 28, 2019 |
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