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ABILIFY
ABILIFY - 59148-006-92 - (ARIPIPRAZOLE)
Drug Information of ABILIFY
| Product NDC: | 59148-006 |
| Proprietary Name: | ABILIFY |
| Non Proprietary Name: | ARIPIPRAZOLE |
| Active Ingredient(s): | 2 mg/1 & nbsp; ARIPIPRAZOLE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ABILIFY
| Product NDC: | 59148-006 |
| Labeler Name: | Otsuka America Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021436 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20021115 |
Package Information of ABILIFY
| Package NDC: | 59148-006-92 |
| Package Description: | 7 TABLET in 1 BLISTER PACK (59148-006-92) |
NDC Information of ABILIFY
| NDC Code | 59148-006-92 |
| Proprietary Name | ABILIFY |
| Package Description | 7 TABLET in 1 BLISTER PACK (59148-006-92) |
| Product NDC | 59148-006 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ARIPIPRAZOLE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20021115 |
| Marketing Category Name | NDA |
| Labeler Name | Otsuka America Pharmaceutical, Inc. |
| Substance Name | ARIPIPRAZOLE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC] |
