NDC 71335-0165 – Duloxetine Delayed-Release
Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release Pellets · Oral
Product NDC71335-0165
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 20 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0165-1 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0165-1) | May 3, 2018 |
| 71335-0165-2 | 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0165-2) | Jul 12, 2018 |
| 71335-0165-3 | 28 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0165-3) | Dec 27, 2021 |
| 71335-0165-4 | 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0165-4) | May 24, 2018 |
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