NDC 71335-0392 – Duloxetine Delayed-Release
Duloxetine Hydrochloride 30 mg/1 · Capsule, Delayed Release Pellets · Oral
Product NDC71335-0392
Product details
- Brand name
- Duloxetine Delayed-Release
- Generic name
- Duloxetine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing category
- ANDA · ANDA203088
- Marketed since
- June 11, 2014
- 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 |
|---|---|---|
| 71335-0392-1 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-1) | Mar 12, 2018 |
| 71335-0392-2 | 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-2) | Mar 22, 2018 |
| 71335-0392-3 | 28 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-3) | May 29, 2024 |
| 71335-0392-4 | 6 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-4) | Nov 8, 2018 |
| 71335-0392-5 | 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-5) | Mar 27, 2018 |
| 71335-0392-6 | 15 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-6) | Feb 18, 2019 |
| 71335-0392-7 | 180 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-7) | Jul 23, 2019 |
| 71335-0392-8 | 120 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-8) | May 29, 2024 |
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