NDC 71335-0924 – Fluoxetine
Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral
Product NDC71335-0924
Product details
- Brand name
- Fluoxetine
- Generic name
- Fluoxetine
- Labeler
- Bryant Ranch Prepack
- 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 (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0924-1 | 30 CAPSULE in 1 BOTTLE (71335-0924-1) | Aug 31, 2018 |
| 71335-0924-2 | 100 CAPSULE in 1 BOTTLE (71335-0924-2) | Dec 14, 2018 |
| 71335-0924-3 | 60 CAPSULE in 1 BOTTLE (71335-0924-3) | Apr 5, 2019 |
| 71335-0924-4 | 15 CAPSULE in 1 BOTTLE (71335-0924-4) | Sep 21, 2022 |
| 71335-0924-5 | 56 CAPSULE in 1 BOTTLE (71335-0924-5) | Sep 21, 2022 |
| 71335-0924-6 | 28 CAPSULE in 1 BOTTLE (71335-0924-6) | Sep 21, 2022 |
| 71335-0924-7 | 90 CAPSULE in 1 BOTTLE (71335-0924-7) | Sep 5, 2018 |
| 71335-0924-8 | 120 CAPSULE in 1 BOTTLE (71335-0924-8) | Sep 21, 2022 |
| 71335-0924-9 | 45 CAPSULE in 1 BOTTLE (71335-0924-9) | Sep 21, 2022 |
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