Strattera is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Carilion Materials Management. The primary component is Atomoxetine Hydrochloride.
| Product ID | 68151-4486_5abe983f-099f-43c0-a0d3-d7afbdf115f8 |
| NDC | 68151-4486 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Strattera |
| Generic Name | Atomoxetine Hydrochloride |
| Dosage Form | Capsule |
| Route of Administration | ORAL |
| Marketing Start Date | 2003-01-10 |
| Marketing Category | NDA / NDA |
| Application Number | NDA021411 |
| Labeler Name | Carilion Materials Management |
| Substance Name | ATOMOXETINE HYDROCHLORIDE |
| Active Ingredient Strength | 25 mg/1 |
| Pharm Classes | Norepinephrine Reuptake Inhibitor [EPC],Norepinephrine Uptake Inhibitors [MoA] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 2003-01-10 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA021411 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2003-01-10 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| ATOMOXETINE HYDROCHLORIDE | 25 mg/1 |
| SPL SET ID: | 2da85bec-890d-477a-b347-767eabb27f9c |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0002-3227 | Strattera | Atomoxetine hydrochloride |
| 0002-3228 | Strattera | Atomoxetine hydrochloride |
| 0002-3229 | Strattera | Atomoxetine hydrochloride |
| 0002-3238 | Strattera | Atomoxetine hydrochloride |
| 0002-3239 | Strattera | Atomoxetine hydrochloride |
| 0002-3250 | Strattera | Atomoxetine hydrochloride |
| 0002-3251 | Strattera | Atomoxetine hydrochloride |
| 49999-636 | Strattera | Atomoxetine |
| 68151-4486 | Strattera | Strattera |
| 68151-4487 | Strattera | Strattera |
| 68151-4484 | Strattera | Strattera |
| 68151-4485 | Strattera | Strattera |
| 68151-4488 | Strattera | Strattera |
| 64725-3228 | Strattera | Strattera |
| 0781-2260 | Atomoxetine hydrochloride | Atomoxetine hydrochloride |
| 0781-2261 | Atomoxetine hydrochloride | Atomoxetine hydrochloride |
| 0781-2262 | Atomoxetine hydrochloride | Atomoxetine hydrochloride |
| 0781-2263 | Atomoxetine hydrochloride | Atomoxetine hydrochloride |
| 0781-2264 | Atomoxetine hydrochloride | Atomoxetine hydrochloride |
| 0781-2265 | Atomoxetine hydrochloride | Atomoxetine hydrochloride |
| 0781-2266 | Atomoxetine hydrochloride | Atomoxetine hydrochloride |
| 50090-4235 | Atomoxetine Hydrochloride | atomoxetine hydrochloride |
| 50090-4236 | Atomoxetine Hydrochloride | atomoxetine hydrochloride |
| 50090-4237 | Atomoxetine Hydrochloride | atomoxetine hydrochloride |
| 50090-4243 | Atomoxetine Hydrochloride | atomoxetine hydrochloride |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() STRATTERA 76306506 2727937 Live/Registered |
Eli Lilly and Company 2001-08-29 |
![]() STRATTERA 75577404 not registered Dead/Abandoned |
Eli Lilly and Company 1998-10-26 |