NDC 47335-618 – Drizalma Sprinkle
Duloxetine Hydrochloride 40 mg/1 · Capsule, Delayed Release · Oral
Product NDC47335-618
Product details
- Brand name
- Drizalma Sprinkle
- Generic name
- Duloxetine
- Labeler
- SUN PHARMACEUTICAL INDUSTRIES, INC.
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- NDA · NDA212516
- Marketed since
- June 10, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 40 mg/1
Uses, dosage, side effects and warnings for Drizalma Sprinkle →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 47335-618-10 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-618-10) | Jun 10, 2024 |
| 47335-618-30 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-618-30) | Jun 10, 2024 |
| 47335-618-60 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-618-60) | Jun 10, 2024 |
| 47335-618-90 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-618-90) | Jun 10, 2024 |
Other Drizalma Sprinkle products
- 47335-616 Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release · SUN PHARMACEUTICAL INDUSTRIES, INC.
- 47335-617 Duloxetine Hydrochloride 30 mg/1 · Capsule, Delayed Release · SUN PHARMACEUTICAL INDUSTRIES, INC.
- 47335-619 Duloxetine Hydrochloride 60 mg/1 · Capsule, Delayed Release · SUN PHARMACEUTICAL INDUSTRIES, INC.