NDC 16714-114 – Fluoxetine hydrochloride
Fluoxetine Hydrochloride 60 mg/1 · Tablet, Film Coated · Oral, Oral
Product NDC16714-114
Product details
- Brand name
- Fluoxetine hydrochloride
- Generic name
- Fluoxetine hydrochloride
- Labeler
- NorthStar Rx LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral, Oral
- Marketing category
- ANDA · ANDA211721
- Marketed since
- September 18, 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 16714-114-01 | 30 TABLET, FILM COATED in 1 BOTTLE (16714-114-01) | Sep 18, 2019 |
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