NDC 71335-2567 – Duloxetine
Duloxetine Hydrochloride 60 mg/1 · Capsule, Delayed Release · Oral
Product NDC71335-2567
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090694
- Marketed since
- December 11, 2013
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 60 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2567-1 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2567-1) | Feb 5, 2025 |
| 71335-2567-2 | 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2567-2) | Feb 5, 2025 |
| 71335-2567-3 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2567-3) | Feb 5, 2025 |
| 71335-2567-4 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2567-4) | Feb 5, 2025 |
| 71335-2567-5 | 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2567-5) | Feb 5, 2025 |
| 71335-2567-6 | 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2567-6) | Feb 5, 2025 |
| 71335-2567-7 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2567-7) | Feb 5, 2025 |
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