Duloxetine Delayed-Release 71335-0392
Generic: Duloxetine Hydrochloride
Product NDC
71335-0392- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 11, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA203088
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Duloxetine Hydrochloride | 30 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(8)
30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-1)
60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-2)
28 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-3)
6 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-4)
90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-5)
15 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-6)
180 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-7)
120 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-8)