NDC 71610-736 – Duloxetine Delayed-Release
Duloxetine Hydrochloride 30 mg/1 · Capsule, Delayed Release Pellets · Oral
Product NDC71610-736
Product details
- Brand name
- Duloxetine Delayed-Release
- Generic name
- Duloxetine Hydrochloride
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Dosage form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing category
- ANDA · ANDA203088
- Marketed since
- June 11, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 30 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 71610-736-42 | 1800 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-736-42) | Sep 15, 2023 |
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