NDC 59651-279 – Duloxetine
Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release · Oral
Product NDC59651-279
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- 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 20 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 59651-279-60 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-279-60) | Dec 11, 2013 |
| 59651-279-78 | 10 BLISTER PACK in 1 CARTON (59651-279-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (59651-279-10) | Dec 11, 2013 |
| 59651-279-99 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-279-99) | Dec 11, 2013 |
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