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Fluoxetine hydrochloride
Fluoxetine hydrochloride - 55111-284-48 - (Fluoxetine Hydrochloride)
Drug Information of Fluoxetine hydrochloride
| Product NDC: | 55111-284 |
| Proprietary Name: | Fluoxetine hydrochloride |
| Non Proprietary Name: | Fluoxetine Hydrochloride |
| Active Ingredient(s): | 90 mg/1 & nbsp; Fluoxetine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, DELAYED RELEASE PELLETS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluoxetine hydrochloride
| Product NDC: | 55111-284 |
| Labeler Name: | Dr.Reddy's Laboratories Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078572 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100324 |
Package Information of Fluoxetine hydrochloride
| Package NDC: | 55111-284-48 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (55111-284-48) > 4 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK |
NDC Information of Fluoxetine hydrochloride
| NDC Code | 55111-284-48 |
| Proprietary Name | Fluoxetine hydrochloride |
| Package Description | 1 BLISTER PACK in 1 CARTON (55111-284-48) > 4 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK |
| Product NDC | 55111-284 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluoxetine Hydrochloride |
| Dosage Form Name | CAPSULE, DELAYED RELEASE PELLETS |
| Route Name | ORAL |
| Start Marketing Date | 20100324 |
| Marketing Category Name | ANDA |
| Labeler Name | Dr.Reddy's Laboratories Limited |
| Substance Name | FLUOXETINE HYDROCHLORIDE |
| Strength Number | 90 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
