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Fluoxetine Hydrochloride
Fluoxetine Hydrochloride - 55289-610-28 - (Fluoxetine Hydrochloride)
Drug Information of Fluoxetine Hydrochloride
| Product NDC: | 55289-610 |
| Proprietary Name: | Fluoxetine Hydrochloride |
| 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 Fluoxetine Hydrochloride
| Product NDC: | 55289-610 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075049 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020129 |
Package Information of Fluoxetine Hydrochloride
| Package NDC: | 55289-610-28 |
| Package Description: | 28 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (55289-610-28) > 14 CAPSULE in 1 BOTTLE, PLASTIC (55289-610-14) |
NDC Information of Fluoxetine Hydrochloride
| NDC Code | 55289-610-28 |
| Proprietary Name | Fluoxetine Hydrochloride |
| Package Description | 28 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (55289-610-28) > 14 CAPSULE in 1 BOTTLE, PLASTIC (55289-610-14) |
| Product NDC | 55289-610 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluoxetine Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20020129 |
| Marketing Category Name | ANDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | FLUOXETINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
