NDC 43547-379 – Duloxetine
Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release · Oral
Product NDC43547-379
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine
- Labeler
- Solco Healthcare US, LLC
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA206653
- Marketed since
- January 20, 2016
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 20 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 43547-379-03 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (43547-379-03) | Jan 20, 2016 |
| 43547-379-06 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (43547-379-06) | Jan 20, 2016 |
| 43547-379-09 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (43547-379-09) | Jan 20, 2016 |
| 43547-379-11 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (43547-379-11) | Jan 20, 2016 |
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