NDC 70518-0417 – Fluoxetine
Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral
Product NDC70518-0417
Product details
- Brand name
- Fluoxetine
- Generic name
- Fluoxetine Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA078619
- Marketed since
- April 10, 2017
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Fluoxetine Hydrochloride 20 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70518-0417-1 | 30 CAPSULE in 1 BLISTER PACK (70518-0417-1) | Apr 14, 2017 |
| 70518-0417-2 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-0417-2) | Apr 20, 2017 |
| 70518-0417-3 | 30 CAPSULE in 1 BOTTLE, PLASTIC (70518-0417-3) | Apr 26, 2017 |
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