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Cymbalta
Cymbalta - 0002-3270-33 - (Duloxetine hydrochloride)
Drug Information of Cymbalta
| Product NDC: | 0002-3270 |
| Proprietary Name: | Cymbalta |
| Non Proprietary Name: | Duloxetine hydrochloride |
| Active Ingredient(s): | 60 mg/1 & nbsp; Duloxetine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cymbalta
| Product NDC: | 0002-3270 |
| Labeler Name: | Eli Lilly and Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021427 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100115 |
Package Information of Cymbalta
| Package NDC: | 0002-3270-33 |
| Package Description: | 100 BLISTER PACK in 1 CARTON (0002-3270-33) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0002-3270-01) |
NDC Information of Cymbalta
| NDC Code | 0002-3270-33 |
| Proprietary Name | Cymbalta |
| Package Description | 100 BLISTER PACK in 1 CARTON (0002-3270-33) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0002-3270-01) |
| Product NDC | 0002-3270 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Duloxetine hydrochloride |
| Dosage Form Name | CAPSULE, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100115 |
| Marketing Category Name | NDA |
| Labeler Name | Eli Lilly and Company |
| Substance Name | DULOXETINE HYDROCHLORIDE |
| Strength Number | 60 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
