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FLUOXETINE
FLUOXETINE - 23155-029-10 - (FLUOXETINE)
Drug Information of FLUOXETINE
| Product NDC: | 23155-029 |
| Proprietary Name: | FLUOXETINE |
| Non Proprietary Name: | FLUOXETINE |
| Active Ingredient(s): | 20 mg/1 & nbsp; FLUOXETINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FLUOXETINE
| Product NDC: | 23155-029 |
| Labeler Name: | Heritage Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201336 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120629 |
Package Information of FLUOXETINE
| Package NDC: | 23155-029-10 |
| Package Description: | 1000 CAPSULE in 1 BOTTLE (23155-029-10) |
NDC Information of FLUOXETINE
| NDC Code | 23155-029-10 |
| Proprietary Name | FLUOXETINE |
| Package Description | 1000 CAPSULE in 1 BOTTLE (23155-029-10) |
| Product NDC | 23155-029 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FLUOXETINE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120629 |
| Marketing Category Name | ANDA |
| Labeler Name | Heritage Pharmaceuticals Inc. |
| Substance Name | FLUOXETINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
