| NDC Code | 71610-739-74 |
|---|
| Package Description | 500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-739-74) |
|---|
| Product NDC | 71610-739 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Duloxetine |
|---|
| Proprietary Name Suffix | Delayed-release |
|---|
| Non-Proprietary Name | Duloxetine Hydrochloride |
|---|
| Dosage Form | CAPSULE, DELAYED RELEASE PELLETS |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20140611 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA203088 |
|---|
| Manufacturer | Aphena Pharma Solutions - Tennessee, LLC |
|---|
| Substance Name | DULOXETINE HYDROCHLORIDE |
|---|
| Strength | 20 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC] |
|---|