NDC 63187-735 – Duloxetine Delayed-release
Duloxetine Hydrochloride 60 mg/1 · Capsule, Delayed Release Pellets · Oral
Product NDC63187-735
Product details
- Brand name
- Duloxetine Delayed-release
- Generic name
- Duloxetine Hydrochloride
- Labeler
- Proficient Rx LP
- 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 60 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 63187-735-30 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-735-30) | Jul 1, 2016 |
| 63187-735-60 | 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-735-60) | Jul 1, 2016 |
| 63187-735-90 | 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-735-90) | Jul 1, 2016 |
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