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Fluoxetine
Fluoxetine - 0121-0721-04 - (FLUOXETINE HYDROCHLORIDE)
Drug Information of Fluoxetine
| Product NDC: | 0121-0721 |
| Proprietary Name: | Fluoxetine |
| Non Proprietary Name: | FLUOXETINE HYDROCHLORIDE |
| Active Ingredient(s): | 20 mg/5mL & nbsp; FLUOXETINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluoxetine
| Product NDC: | 0121-0721 |
| Labeler Name: | Pharmaceutical Associates, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076015 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020130 |
Package Information of Fluoxetine
| Package NDC: | 0121-0721-04 |
| Package Description: | 120 mL in 1 BOTTLE (0121-0721-04) |
NDC Information of Fluoxetine
| NDC Code | 0121-0721-04 |
| Proprietary Name | Fluoxetine |
| Package Description | 120 mL in 1 BOTTLE (0121-0721-04) |
| Product NDC | 0121-0721 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FLUOXETINE HYDROCHLORIDE |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20020130 |
| Marketing Category Name | ANDA |
| Labeler Name | Pharmaceutical Associates, Inc. |
| Substance Name | FLUOXETINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
