NDC 50771-203 – Duloxetine Hydrochloride
Duloxetine Hydrochloride 60 mg/1 · Capsule, Delayed Release Pellets · Oral
Product NDC50771-203
Product details
- Brand name
- Duloxetine Hydrochloride
- Generic name
- Duloxetine Hydrochloride
- Labeler
- Yaopharma Co., Ltd.
- Dosage form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing category
- ANDA · ANDA207219
- Marketed since
- January 1, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 60 mg/1
Uses, dosage, side effects and warnings for Duloxetine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 50771-203-01 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (50771-203-01) | Jan 1, 2024 |
| 50771-203-02 | 500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (50771-203-02) | Jan 1, 2024 |
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