| NDC Code | 51991-747-10 |
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| Package Description | 1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-747-10) |
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| Product NDC | 51991-747 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Duloxetine |
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| Proprietary Name Suffix | Delayed-release |
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| Non-Proprietary Name | Duloxetine Hydrochloride |
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| Dosage Form | CAPSULE, DELAYED RELEASE PELLETS |
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| Usage | ORAL |
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| Start Marketing Date | 20140611 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203088 |
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| Manufacturer | Breckenridge Pharmaceutical, Inc. |
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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 Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC] |
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