NDC 70247-013 – Duloxetine
Duloxetine Hydrochloride 30 mg/1 · Capsule, Delayed Release · Oral
Product NDC70247-013
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 30 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70247-013-03 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70247-013-03) | May 8, 2018 |
| 70247-013-09 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70247-013-09) | May 8, 2018 |
| 70247-013-10 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70247-013-10) | May 8, 2018 |
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