NDC 68788-7935 – Duloxetine
Duloxetine Hydrochloride 30 mg/1 · Capsule, Delayed Release · Oral
Product NDC68788-7935
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA208706
- Marketed since
- June 15, 2021
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 30 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68788-7935-3 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7935-3) | Jun 15, 2021 |
| 68788-7935-6 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7935-6) | Jun 15, 2021 |
| 68788-7935-9 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7935-9) | Jun 15, 2021 |
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