NDC 68788-7897 – Duloxetine Delayed-Release
Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release Pellets · Oral
Product NDC68788-7897
Product details
- Brand name
- Duloxetine Delayed-Release
- Generic name
- Duloxetine Hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing category
- ANDA · ANDA203088
- Marketed since
- May 14, 2021
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 20 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68788-7897-3 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7897-3) | May 14, 2021 |
| 68788-7897-6 | 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7897-6) | May 14, 2021 |
| 68788-7897-9 | 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7897-9) | May 14, 2021 |
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