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Atomoxetine Hydrochloride
Atomoxetine Hydrochloride - 47335-817-08 - (Atomoxetine Hydrochloride)
Drug Information of Atomoxetine Hydrochloride
| Product NDC: | 47335-817 |
| Proprietary Name: | Atomoxetine Hydrochloride |
| Non Proprietary Name: | Atomoxetine Hydrochloride |
| Active Ingredient(s): | 40 mg/1 & nbsp; Atomoxetine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Atomoxetine Hydrochloride
| Product NDC: | 47335-817 |
| Labeler Name: | Sun Pharma Global FZE |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079020 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101005 |
Package Information of Atomoxetine Hydrochloride
| Package NDC: | 47335-817-08 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (47335-817-08) |
NDC Information of Atomoxetine Hydrochloride
| NDC Code | 47335-817-08 |
| Proprietary Name | Atomoxetine Hydrochloride |
| Package Description | 100 CAPSULE in 1 BOTTLE (47335-817-08) |
| Product NDC | 47335-817 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Atomoxetine Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20101005 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharma Global FZE |
| Substance Name | ATOMOXETINE HYDROCHLORIDE |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Norepinephrine Reuptake Inhibitor [EPC],Norepinephrine Uptake Inhibitors [MoA] |
