Home
>
National Drug Code (NDC)
>
Prozac
Prozac - 0002-3004-75 - (Fluoxetine hydrochloride)
Drug Information of Prozac
| Product NDC: | 0002-3004 |
| Proprietary Name: | Prozac |
| Non Proprietary Name: | Fluoxetine hydrochloride |
| Active Ingredient(s): | 90 mg/1 & nbsp; Fluoxetine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prozac
| Product NDC: | 0002-3004 |
| Labeler Name: | Eli Lilly and Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021235 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20010316 |
Package Information of Prozac
| Package NDC: | 0002-3004-75 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (0002-3004-75) > 2 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK |
NDC Information of Prozac
| NDC Code | 0002-3004-75 |
| Proprietary Name | Prozac |
| Package Description | 2 BLISTER PACK in 1 CARTON (0002-3004-75) > 2 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK |
| Product NDC | 0002-3004 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluoxetine hydrochloride |
| Dosage Form Name | CAPSULE, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20010316 |
| Marketing Category Name | NDA |
| Labeler Name | Eli Lilly and Company |
| Substance Name | FLUOXETINE HYDROCHLORIDE |
| Strength Number | 90 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
