NDC 71335-1482 – Fluoxetine
Fluoxetine Hydrochloride 40 mg/1 · Capsule · Oral
Product NDC71335-1482
Product details
- Brand name
- Fluoxetine
- Generic name
- Fluoxetine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA204597
- Marketed since
- March 16, 2015
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Fluoxetine Hydrochloride 40 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1482-1 | 30 CAPSULE in 1 BOTTLE (71335-1482-1) | Feb 12, 2020 |
| 71335-1482-2 | 60 CAPSULE in 1 BOTTLE (71335-1482-2) | Feb 18, 2021 |
| 71335-1482-3 | 100 CAPSULE in 1 BOTTLE (71335-1482-3) | Apr 21, 2020 |
| 71335-1482-4 | 90 CAPSULE in 1 BOTTLE (71335-1482-4) | Jan 17, 2020 |
| 71335-1482-5 | 28 CAPSULE in 1 BOTTLE (71335-1482-5) | Jul 15, 2024 |
| 71335-1482-6 | 180 CAPSULE in 1 BOTTLE (71335-1482-6) | Jul 15, 2024 |
| 71335-1482-7 | 120 CAPSULE in 1 BOTTLE (71335-1482-7) | Jul 15, 2024 |
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