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Strattera
Strattera - 0002-5800-35 - (Atomoxetine hydrochloride)
Drug Information of Strattera
| Product NDC: | 0002-5800 |
| Proprietary Name: | Strattera |
| Non Proprietary Name: | Atomoxetine hydrochloride |
| Active Ingredient(s): | & nbsp; Atomoxetine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Strattera
| Product NDC: | 0002-5800 |
| Labeler Name: | Eli Lilly and Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021411 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090316 |
Package Information of Strattera
| Package NDC: | 0002-5800-35 |
| Package Description: | 1 KIT in 1 BLISTER PACK (0002-5800-35) |
NDC Information of Strattera
| NDC Code | 0002-5800-35 |
| Proprietary Name | Strattera |
| Package Description | 1 KIT in 1 BLISTER PACK (0002-5800-35) |
| Product NDC | 0002-5800 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Atomoxetine hydrochloride |
| Dosage Form Name | KIT |
| Route Name | ORAL |
| Start Marketing Date | 20090316 |
| Marketing Category Name | NDA |
| Labeler Name | Eli Lilly and Company |
| Substance Name | |
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