NDC Code | 55111-609-81 |
Package Description | 3 BLISTER PACK in 1 CARTON (55111-609-81) > 10 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK (55111-609-79) |
Product NDC | 55111-609 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Duloxetine |
Non-Proprietary Name | Duloxetine |
Dosage Form | CAPSULE, DELAYED RELEASE PELLETS |
Usage | ORAL |
Start Marketing Date | 20140618 |
Marketing Category Name | ANDA |
Application Number | ANDA090723 |
Manufacturer | Dr. Reddy's Laboratories Limited |
Substance Name | DULOXETINE HYDROCHLORIDE |
Strength | 30 |
Strength Unit | mg/1 |
Pharmacy Classes | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |