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Abilify
Abilify - 49999-817-30 - (Aripiprazole)
Drug Information of Abilify
| Product NDC: | 49999-817 |
| Proprietary Name: | Abilify |
| Non Proprietary Name: | Aripiprazole |
| Active Ingredient(s): | 15 mg/1 & nbsp; Aripiprazole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Abilify
| Product NDC: | 49999-817 |
| Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021436 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100603 |
Package Information of Abilify
| Package NDC: | 49999-817-30 |
| Package Description: | 30 TABLET in 1 BOX (49999-817-30) |
NDC Information of Abilify
| NDC Code | 49999-817-30 |
| Proprietary Name | Abilify |
| Package Description | 30 TABLET in 1 BOX (49999-817-30) |
| Product NDC | 49999-817 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Aripiprazole |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100603 |
| Marketing Category Name | NDA |
| Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
| Substance Name | ARIPIPRAZOLE |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC] |
