NDC 43063-712 – Fluoxetine
Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral
Product NDC43063-712
Product details
- Brand name
- Fluoxetine
- Generic name
- Fluoxetine Hydrochloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA078619
- Marketed since
- January 31, 2008
- Marketing end
- November 30, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Fluoxetine Hydrochloride 20 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 43063-712-21 | 21 CAPSULE in 1 BOTTLE, PLASTIC (43063-712-21) | Jan 31, 2017 |
| 43063-712-30 | 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-712-30) | Oct 3, 2016 |
| 43063-712-60 | 60 CAPSULE in 1 BOTTLE, PLASTIC (43063-712-60) | Aug 24, 2018 |
| 43063-712-90 | 90 CAPSULE in 1 BOTTLE, PLASTIC (43063-712-90) | Jan 31, 2017 |
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