NDC 71205-178 – Fluoxetine
Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral
Product NDC71205-178
Product details
- Brand name
- Fluoxetine
- Generic name
- Fluoxetine
- Labeler
- Proficient Rx LP
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA076001
- Marketed since
- January 29, 2002
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Fluoxetine Hydrochloride 20 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 71205-178-30 | 30 CAPSULE in 1 BOTTLE (71205-178-30) | Jan 29, 2002 |
| 71205-178-60 | 60 CAPSULE in 1 BOTTLE (71205-178-60) | Jan 29, 2002 |
| 71205-178-90 | 90 CAPSULE in 1 BOTTLE (71205-178-90) | Jan 29, 2002 |
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