| NDC Code | 51991-750-05 |
|---|
| Package Description | 500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-05) |
|---|
| Product NDC | 51991-750 |
|---|
| 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 | 20180521 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA203088 |
|---|
| Manufacturer | Breckenridge Pharmaceutical, Inc. |
|---|
| Substance Name | DULOXETINE HYDROCHLORIDE |
|---|
| Strength | 40 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC] |
|---|