NDC 70518-1054 – Duloxetine
Duloxetine Hydrochloride 30 mg/1 · Capsule, Delayed Release · Oral
Product NDC70518-1054
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA208706
- Marketed since
- March 9, 2018
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 30 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 70518-1054-0 | 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1054-0) | Mar 9, 2018 |
| 70518-1054-6 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1054-6) | Jun 9, 2021 |
| 70518-1054-7 | 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1054-7) | Jun 25, 2021 |
| 70518-1054-9 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1054-9) | Dec 2, 2021 |
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