NDC 71335-2017 – Duloxetine
Duloxetine Hydrochloride 30 mg/1 · Capsule, Delayed Release · Oral
Product NDC71335-2017
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, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 30 mg/1
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2017-1 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-1) | Feb 10, 2022 |
| 71335-2017-2 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-2) | Feb 10, 2022 |
| 71335-2017-3 | 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-3) | Feb 10, 2022 |
| 71335-2017-4 | 6 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-4) | Feb 10, 2022 |
| 71335-2017-5 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-5) | Feb 10, 2022 |
| 71335-2017-6 | 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-6) | Feb 10, 2022 |
| 71335-2017-7 | 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-7) | Feb 10, 2022 |
| 71335-2017-8 | 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-8) | Feb 10, 2022 |
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