NDC 71205-525 – Duloxetine
Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release Pellets · Oral
Product NDC71205-525
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine
- Labeler
- Proficient Rx LP
- Dosage form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing category
- ANDA · ANDA090776
- Marketed since
- December 17, 2013
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 20 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 71205-525-30 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-30) | Jan 22, 2021 |
| 71205-525-60 | 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-60) | Jan 22, 2021 |
| 71205-525-90 | 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-90) | Jan 22, 2021 |
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