Product NDC: | 59148-019 |
Proprietary Name: | ABILIFY MAINTENA KIT |
Non Proprietary Name: | aripiprazole |
Active Ingredient(s): | 400 mg/2mL & nbsp; aripiprazole |
Administration Route(s): | INTRAMUSCULAR |
Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59148-019 |
Labeler Name: | Otsuka America Pharmaceutical, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA202971 |
Marketing Category: | NDA |
Start Marketing Date: | 20120901 |
Package NDC: | 59148-019-71 |
Package Description: | 1 VIAL in 1 KIT (59148-019-71) > 2 mL in 1 VIAL |
NDC Code | 59148-019-71 |
Proprietary Name | ABILIFY MAINTENA KIT |
Package Description | 1 VIAL in 1 KIT (59148-019-71) > 2 mL in 1 VIAL |
Product NDC | 59148-019 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | aripiprazole |
Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION, EXTENDED RELEASE |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 20120901 |
Marketing Category Name | NDA |
Labeler Name | Otsuka America Pharmaceutical, Inc. |
Substance Name | ARIPIPRAZOLE |
Strength Number | 400 |
Strength Unit | mg/2mL |
Pharmaceutical Classes | Atypical Antipsychotic [EPC] |