NDC 71335-3062 – Duloxetine
Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release · Oral
Product NDC71335-3062
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA208706
- Marketed since
- March 16, 2017
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 20 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 71335-3062-1 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-3062-1) | Feb 6, 2026 |
| 71335-3062-2 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-3062-2) | Feb 6, 2026 |
| 71335-3062-3 | 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-3062-3) | Feb 6, 2026 |
| 71335-3062-4 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-3062-4) | Feb 6, 2026 |
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