NDC 16714-722 – Fluoxetine
Fluoxetine Hydrochloride 40 mg/1 · Capsule · Oral
Product NDC16714-722
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 40 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 16714-722-02 | 100 CAPSULE in 1 BOTTLE (16714-722-02) | Jan 31, 2008 |
| 16714-722-03 | 500 CAPSULE in 1 BOTTLE (16714-722-03) | Jan 31, 2008 |
| 16714-722-04 | 1000 CAPSULE in 1 BOTTLE (16714-722-04) | Jan 31, 2008 |
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