NDC 0002-3235 – Cymbalta
Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release · Oral
Product NDC0002-3235
Product details
- Brand name
- Cymbalta
- Generic name
- Duloxetine hydrochloride
- Labeler
- Eli Lilly and Company
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- NDA · NDA021427
- Marketed since
- August 24, 2004
- Marketing end
- October 2, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 20 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0002-3235-60 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0002-3235-60) | Aug 24, 2004 |