NDC 68001-368 – Duloxetine Delayed-Release
Duloxetine Hydrochloride 40 mg/1 · Capsule, Delayed Release Pellets · Oral
Product NDC68001-368
Product details
- Brand name
- Duloxetine Delayed-Release
- Generic name
- Duloxetine Hydrochloride
- Labeler
- BluePoint Laboratories
- Dosage form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing category
- ANDA · ANDA203088
- Marketed since
- May 21, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 40 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68001-368-04 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68001-368-04) | May 21, 2018 |
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