NDC 0093-7198 – Fluoxetine
Fluoxetine Hydrochloride 40 mg/1 · Capsule · Oral
Product NDC0093-7198
Product details
- Brand name
- Fluoxetine
- Generic name
- Fluoxetine
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA075452
- Marketed since
- January 30, 2002
- 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 |
|---|---|---|
| 0093-7198-01 | 100 CAPSULE in 1 BOTTLE (0093-7198-01) | Sep 8, 2008 |
| 0093-7198-05 | 500 CAPSULE in 1 BOTTLE (0093-7198-05) | Sep 23, 2008 |
| 0093-7198-56 | 30 CAPSULE in 1 BOTTLE (0093-7198-56) | Jan 30, 2002 |
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