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Fluoxetine Hydrochloride
Fluoxetine Hydrochloride - 49884-735-10 - (fluoxetine hydrochloride)
Drug Information of Fluoxetine Hydrochloride
| Product NDC: | 49884-735 |
| 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): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluoxetine Hydrochloride
| Product NDC: | 49884-735 |
| Labeler Name: | Par Pharmaceutical, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075755 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100113 |
Package Information of Fluoxetine Hydrochloride
| Package NDC: | 49884-735-10 |
| Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49884-735-10) |
NDC Information of Fluoxetine Hydrochloride
| NDC Code | 49884-735-10 |
| Proprietary Name | Fluoxetine Hydrochloride |
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49884-735-10) |
| Product NDC | 49884-735 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluoxetine hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100113 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical, Inc |
| Substance Name | FLUOXETINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
