aripiprazole
- Product NDC
- 82804-235
- 11-digit product format
- 828040235
- Labeler code
- 82804
- Product ID
- 82804-235_2c2b0172-b186-4be4-a002-4a26adf120c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- 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 |
|---|
| 82804-235-90 | 82804023590 | 90 TABLET in 1 BOTTLE (82804-235-90) | 90 tablet | 2025-08-19 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| aripiprazole | Proficient Rx LP | 2025-08-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |