NDC 71335-2537 – Duloxetine
Duloxetine Hydrochloride 30 mg/1 · Capsule, Delayed Release · Oral
Product NDC71335-2537
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, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 30 mg/1
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2537-1 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-1) | Dec 10, 2024 |
| 71335-2537-2 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-2) | Dec 10, 2024 |
| 71335-2537-3 | 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-3) | Dec 10, 2024 |
| 71335-2537-4 | 6 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-4) | Dec 10, 2024 |
| 71335-2537-5 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-5) | Dec 10, 2024 |
| 71335-2537-6 | 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-6) | Dec 10, 2024 |
| 71335-2537-7 | 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-7) | Dec 10, 2024 |
| 71335-2537-8 | 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-8) | Dec 10, 2024 |
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