NDC 82009-172 – Duloxetine
Duloxetine Hydrochloride 40 mg/1 · Capsule, Delayed Release · Oral
Product NDC82009-172
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine
- Labeler
- Quallent Pharmaceuticals Health LLC
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA208706
- Marketed since
- July 1, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 40 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 82009-172-30 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-172-30) | Jul 1, 2025 |
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