NDC 16714-721 – Fluoxetine
Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral
Product NDC16714-721
Product details
- Brand name
- Fluoxetine
- Generic name
- Fluoxetine Hydrochloride
- Labeler
- NorthStar Rx LLC
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA078619
- Marketed since
- January 31, 2008
- 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 |
|---|---|---|
| 16714-721-02 | 100 CAPSULE in 1 BOTTLE (16714-721-02) | Jan 31, 2008 |
| 16714-721-03 | 1000 CAPSULE in 1 BOTTLE (16714-721-03) | Jan 31, 2008 |
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