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Atomoxetine hydrochloride
Atomoxetine hydrochloride - 0781-2262-22 - (Atomoxetine hydrochloride)
Drug Information of Atomoxetine hydrochloride
| Product NDC: | 0781-2262 |
| Proprietary Name: | Atomoxetine hydrochloride |
| Non Proprietary Name: | Atomoxetine hydrochloride |
| Active Ingredient(s): | 25 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: | 0781-2262 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079018 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101215 |
Package Information of Atomoxetine hydrochloride
| Package NDC: | 0781-2262-22 |
| Package Description: | 2000 CAPSULE in 1 BOTTLE (0781-2262-22) |
NDC Information of Atomoxetine hydrochloride
| NDC Code | 0781-2262-22 |
| Proprietary Name | Atomoxetine hydrochloride |
| Package Description | 2000 CAPSULE in 1 BOTTLE (0781-2262-22) |
| Product NDC | 0781-2262 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Atomoxetine hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20101215 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | ATOMOXETINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Norepinephrine Reuptake Inhibitor [EPC],Norepinephrine Uptake Inhibitors [MoA] |
