NDC 65841-799 – Duloxetine
Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release · Oral
Product NDC65841-799
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090739
- Marketed since
- May 27, 2014
- 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 |
|---|---|---|
| 65841-799-06 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-799-06) | May 27, 2014 |
| 65841-799-14 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-799-14) | May 27, 2014 |
| 65841-799-16 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-799-16) | May 27, 2014 |
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