NDC 67877-265 – Duloxetine
Duloxetine Hydrochloride 60 mg/1 · Capsule, Delayed Release · Oral
Product NDC67877-265
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA203197
- Marketed since
- May 1, 2012
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 60 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 67877-265-01 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-265-01) | May 1, 2012 |
| 67877-265-10 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-265-10) | May 1, 2012 |
| 67877-265-30 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-265-30) | May 1, 2012 |
| 67877-265-90 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-265-90) | May 1, 2012 |
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