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FLUOXETINE
FLUOXETINE - 49884-872-05 - (fluoxetine hydrochloride)
Drug Information of FLUOXETINE
| Product NDC: | 49884-872 |
| Proprietary Name: | FLUOXETINE |
| Non Proprietary Name: | fluoxetine hydrochloride |
| Active Ingredient(s): | 40 mg/1 & nbsp; fluoxetine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FLUOXETINE
| Product NDC: | 49884-872 |
| Labeler Name: | Par Pharmaceutical Companies, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076922 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081208 |
Package Information of FLUOXETINE
| Package NDC: | 49884-872-05 |
| Package Description: | 500 CAPSULE in 1 BOTTLE (49884-872-05) |
NDC Information of FLUOXETINE
| NDC Code | 49884-872-05 |
| Proprietary Name | FLUOXETINE |
| Package Description | 500 CAPSULE in 1 BOTTLE (49884-872-05) |
| Product NDC | 49884-872 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluoxetine hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20081208 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical Companies, Inc. |
| Substance Name | FLUOXETINE HYDROCHLORIDE |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
