NDC 68788-8362 – Duloxetine Delayed-Release
Duloxetine Hydrochloride 40 mg/1 · Capsule, Delayed Release Pellets · Oral
Product NDC68788-8362
Product details
- Brand name
- Duloxetine Delayed-Release
- Generic name
- Duloxetine Hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing category
- ANDA · ANDA203088
- Marketed since
- February 1, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 40 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8362-0 | 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-0) | Mar 14, 2023 |
| 68788-8362-3 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-3) | Feb 1, 2023 |
| 68788-8362-9 | 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-9) | Feb 1, 2023 |
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