Product NDC: | 59148-016 |
Proprietary Name: | ABILIFY |
Non Proprietary Name: | ARIPIPRAZOLE |
Active Ingredient(s): | 9.75 mg/1.3mL & nbsp; ARIPIPRAZOLE |
Administration Route(s): | INTRAMUSCULAR |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59148-016 |
Labeler Name: | Otsuka America Pharmaceutical, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021866 |
Marketing Category: | NDA |
Start Marketing Date: | 20060920 |
Package NDC: | 59148-016-65 |
Package Description: | 1.3 mL in 1 VIAL (59148-016-65) |
NDC Code | 59148-016-65 |
Proprietary Name | ABILIFY |
Package Description | 1.3 mL in 1 VIAL (59148-016-65) |
Product NDC | 59148-016 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ARIPIPRAZOLE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 20060920 |
Marketing Category Name | NDA |
Labeler Name | Otsuka America Pharmaceutical, Inc. |
Substance Name | ARIPIPRAZOLE |
Strength Number | 9.75 |
Strength Unit | mg/1.3mL |
Pharmaceutical Classes | Atypical Antipsychotic [EPC] |