NDC 16714-113 – Fluoxetine
Fluoxetine Hydrochloride 20 mg/1 · Tablet, Film Coated · Oral
Product NDC16714-113
Product details
- Brand name
- Fluoxetine
- Generic name
- Fluoxetine
- Labeler
- NorthStar Rx LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076006
- Marketed since
- September 18, 2019
- 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 |
|---|---|---|
| 16714-113-01 | 30 TABLET, FILM COATED in 1 BOTTLE (16714-113-01) | Sep 18, 2019 |
| 16714-113-02 | 100 TABLET, FILM COATED in 1 BOTTLE (16714-113-02) | Sep 18, 2019 |
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