aripiprazole
- Product NDC
- 50090-6563
- 11-digit product format
- 500906563
- Labeler code
- 50090
- Product ID
- 50090-6563_864c7f42-f10f-4f87-a3a8-4075a10374d1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA201519
- Marketing category
- ANDA
- Marketing start
- 2015-04-28
- Substance
- ARIPIPRAZOLE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 82VFR53I78 | ARIPIPRAZOLE | 129722-12-9 | ARIPIPRAZOLE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6563-0 | 50090656300 | 30 TABLET in 1 BOTTLE (50090-6563-0) | 30 tablet | 2023-07-18 | No | No | Historical |
| 50090-6563-1 | 50090656301 | 90 TABLET in 1 BOTTLE (50090-6563-1) | 90 tablet | 2023-07-18 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| aripiprazole | A-S Medication Solutions | 2024-06-05 | HUMAN PRESCRIPTION DRUG LABEL | 3 |