NDC 71610-402 – Duloxetine
Duloxetine Hydrochloride 30 mg/1 · Capsule, Delayed Release · Oral
Product NDC71610-402
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine Hydrochloride
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090778
- Marketed since
- December 11, 2013
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 30 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 71610-402-60 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-402-60) | Feb 26, 2020 |
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