NDC 71335-1033 – Fluoxetine
Fluoxetine Hydrochloride 10 mg/1 · Capsule · Oral
Product NDC71335-1033
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, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Fluoxetine Hydrochloride 10 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1033-1 | 30 CAPSULE in 1 BOTTLE (71335-1033-1) | Jan 3, 2019 |
| 71335-1033-2 | 90 CAPSULE in 1 BOTTLE (71335-1033-2) | Jan 3, 2019 |
| 71335-1033-3 | 60 CAPSULE in 1 BOTTLE (71335-1033-3) | Jan 3, 2019 |
| 71335-1033-4 | 120 CAPSULE in 1 BOTTLE (71335-1033-4) | Jan 3, 2019 |
| 71335-1033-5 | 28 CAPSULE in 1 BOTTLE (71335-1033-5) | Jan 3, 2019 |
| 71335-1033-6 | 15 CAPSULE in 1 BOTTLE (71335-1033-6) | Jan 3, 2019 |
| 71335-1033-7 | 100 CAPSULE in 1 BOTTLE (71335-1033-7) | Jan 3, 2019 |
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