NDC 25000-609 – Duloxetine
Duloxetine Hydrochloride 30 mg/1 · Capsule, Delayed Release · Oral
Product NDC25000-609
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine Hydrochloride
- Labeler
- MARKSANS PHARMA LIMITED
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090723
- Marketed since
- May 27, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 30 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 25000-609-03 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (25000-609-03) | May 27, 2022 |
| 25000-609-07 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (25000-609-07) | May 27, 2022 |
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