NDC 70247-012 – duloxetine
Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release · Oral
Product NDC70247-012
Product details
- Brand name
- duloxetine
- Generic name
- Duloxetine
- Labeler
- Qingdao BAHEAL Pharmaceutical Co., Ltd.
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210599
- Marketed since
- May 5, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 20 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70247-012-06 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70247-012-06) | May 8, 2018 |
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