NDC 70518-4440 – Duloxetine
Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release · Oral
Product NDC70518-4440
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090694
- Marketed since
- August 14, 2025
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 20 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 70518-4440-0 | 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-4440-0) | Aug 14, 2025 |
| 70518-4440-1 | 50 POUCH in 1 BOX (70518-4440-1) / 1 CAPSULE, DELAYED RELEASE in 1 POUCH (70518-4440-2) | May 27, 2026 |
| 70518-4440-3 | 100 POUCH in 1 BOX (70518-4440-3) / 1 CAPSULE, DELAYED RELEASE in 1 POUCH (70518-4440-2) | Jun 26, 2026 |
| 70518-4440-4 | 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-4440-4) | Jul 14, 2026 |
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