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Atomoxetine Hydrochloride
Atomoxetine Hydrochloride - 0378-8110-93 - (atomoxetine hydrochloride)
Drug Information of Atomoxetine Hydrochloride
| Product NDC: | 0378-8110 |
| Proprietary Name: | Atomoxetine Hydrochloride |
| Non Proprietary Name: | atomoxetine hydrochloride |
| Active Ingredient(s): | 100 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: | 0378-8110 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079021 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111101 |
Package Information of Atomoxetine Hydrochloride
| Package NDC: | 0378-8110-93 |
| Package Description: | 30 CAPSULE in 1 BOTTLE, PLASTIC (0378-8110-93) |
NDC Information of Atomoxetine Hydrochloride
| NDC Code | 0378-8110-93 |
| Proprietary Name | Atomoxetine Hydrochloride |
| Package Description | 30 CAPSULE in 1 BOTTLE, PLASTIC (0378-8110-93) |
| Product NDC | 0378-8110 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | atomoxetine hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20111101 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | ATOMOXETINE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Norepinephrine Reuptake Inhibitor [EPC],Norepinephrine Uptake Inhibitors [MoA] |
