NDC 68071-3979 – Duloxetine
Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release · Oral
Product NDC68071-3979
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine
- Labeler
- NuCare Pharmaceuticals, Inc.
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA208706
- Marketed since
- March 16, 2017
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 20 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68071-3979-6 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3979-6) | Mar 30, 2026 |
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