NDC 51407-818 – Duloxetine Delayed-Release
Duloxetine Hydrochloride 30 mg/1 · Capsule, Delayed Release Pellets · Oral
Product NDC51407-818
Product details
- Brand name
- Duloxetine Delayed-Release
- Generic name
- Duloxetine Hydrochloride
- Labeler
- Golden State Medical Supply, Inc.
- Dosage form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing category
- ANDA · ANDA203088
- Marketed since
- June 11, 2014
- Marketing end
- December 31, 2027
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 30 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51407-818-30 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51407-818-30) | Jul 12, 2023 |
| 51407-818-90 | 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51407-818-90) | Jul 12, 2023 |
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