Duloxetine Delayed-Release 51991-0750
Generic: Duloxetine Hydrochloride
Product NDC
51991-0750- Manufacturer
- Breckenridge Pharmaceutical, Inc.
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 21, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA203088
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Duloxetine Hydrochloride | 40 mg/1 |
Drug Class
Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Packaging Options(4)
500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-05)
1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-10)
30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-33)
90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-90)