NDC 59651-309 – Fluoxetine
Fluoxetine Hydrochloride 20 mg/1 · Tablet, Film Coated · Oral
Product NDC59651-309
Product details
- Brand name
- Fluoxetine
- Generic name
- Fluoxetine
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA213286
- Marketed since
- April 8, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Fluoxetine Hydrochloride 20 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 59651-309-01 | 100 TABLET, FILM COATED in 1 BOTTLE (59651-309-01) | Apr 8, 2020 |
| 59651-309-30 | 30 TABLET, FILM COATED in 1 BOTTLE (59651-309-30) | Apr 8, 2020 |
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