Aripiprazole 67877-0435
Product NDC
67877-0435- Manufacturer
- Ascend Laboratories, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 27, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA207105
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Aripiprazole | 30 mg/1 |
Drug Class
Atypical Antipsychotic [EPC]Atypical Antipsychotic [EPC]
Packaging Options(4)
100 TABLET in 1 BOTTLE (67877-435-01)
30 TABLET in 1 BOTTLE (67877-435-03)
500 TABLET in 1 BOTTLE (67877-435-05)
10 BLISTER PACK in 1 CARTON (67877-435-38) / 10 TABLET in 1 BLISTER PACK (67877-435-33)