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Fluoxetine
Fluoxetine - 54838-523-40 - (Fluoxetine Hydrochloride)
Drug Information of Fluoxetine
| Product NDC: | 54838-523 |
| Proprietary Name: | Fluoxetine |
| Non Proprietary Name: | Fluoxetine Hydrochloride |
| Active Ingredient(s): | 20 mg/5mL & nbsp; Fluoxetine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluoxetine
| Product NDC: | 54838-523 |
| Labeler Name: | Silarx Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077849 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090827 |
Package Information of Fluoxetine
| Package NDC: | 54838-523-40 |
| Package Description: | 120 mL in 1 BOTTLE, PLASTIC (54838-523-40) |
NDC Information of Fluoxetine
| NDC Code | 54838-523-40 |
| Proprietary Name | Fluoxetine |
| Package Description | 120 mL in 1 BOTTLE, PLASTIC (54838-523-40) |
| Product NDC | 54838-523 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluoxetine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20090827 |
| Marketing Category Name | ANDA |
| Labeler Name | Silarx Pharmaceuticals, Inc |
| Substance Name | FLUOXETINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
