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Prozac
Prozac - 0777-3105-02 - (Fluoxetine hydrochloride)
Drug Information of Prozac
| Product NDC: | 0777-3105 |
| Proprietary Name: | Prozac |
| Non Proprietary Name: | Fluoxetine hydrochloride |
| Active Ingredient(s): | 20 mg/1 & nbsp; Fluoxetine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prozac
| Product NDC: | 0777-3105 |
| Labeler Name: | Dista Products Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018936 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19880201 |
Package Information of Prozac
| Package NDC: | 0777-3105-02 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (0777-3105-02) |
NDC Information of Prozac
| NDC Code | 0777-3105-02 |
| Proprietary Name | Prozac |
| Package Description | 100 CAPSULE in 1 BOTTLE (0777-3105-02) |
| Product NDC | 0777-3105 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluoxetine hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19880201 |
| Marketing Category Name | NDA |
| Labeler Name | Dista Products Company |
| Substance Name | FLUOXETINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
