NDC 43598-566 – Fluoxetine
Fluoxetine Hydrochloride 20 mg/1 · Tablet, Film Coated · Oral
Product NDC43598-566
Product details
- Brand name
- Fluoxetine
- Generic name
- Fluoxetine
- Labeler
- Dr.Reddy's Laboratories Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076006
- Marketed since
- May 8, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Fluoxetine Hydrochloride 20 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 43598-566-01 | 100 TABLET, FILM COATED in 1 BOTTLE (43598-566-01) | May 8, 2018 |
| 43598-566-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (43598-566-10) | May 8, 2018 |
| 43598-566-30 | 30 TABLET, FILM COATED in 1 BOTTLE (43598-566-30) | May 8, 2018 |
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