NDC 87063-704 – Duloxetine
Duloxetine Hydrochloride 40 mg/1 · Capsule, Delayed Release · Oral
Product NDC87063-704
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine
- Labeler
- ASCLEMED USA INC.
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA208706
- Marketed since
- March 25, 2019
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 40 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 87063-704-12 | 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (87063-704-12) | Jul 2, 2026 |
| 87063-704-30 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (87063-704-30) | Jul 2, 2026 |
| 87063-704-60 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (87063-704-60) | Jul 2, 2026 |
| 87063-704-90 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (87063-704-90) | Jul 2, 2026 |
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