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