NDC 50228-421 – Fluoxetine
Fluoxetine Hydrochloride 20 mg/1 · Tablet, Film Coated · Oral
Product NDC50228-421
Product details
- Brand name
- Fluoxetine
- Generic name
- Fluoxetine
- Labeler
- ScieGen Pharmaceuticals, Inc
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA210935
- Marketed since
- March 20, 2019
- 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 |
|---|---|---|
| 50228-421-01 | 100 TABLET, FILM COATED in 1 BOTTLE (50228-421-01) | Mar 20, 2019 |
| 50228-421-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (50228-421-10) | Mar 20, 2019 |
| 50228-421-30 | 30 TABLET, FILM COATED in 1 BOTTLE (50228-421-30) | Mar 20, 2019 |
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