Aripiprazole
- Product NDC
- 50090-7125
- 11-digit product format
- 500907125
- Labeler code
- 50090
- Product ID
- 50090-7125_fc6e3258-1414-499b-853e-8d4809d51b43
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA205064
- Marketing category
- ANDA
- Marketing start
- 2020-10-01
- Substance
- ARIPIPRAZOLE
- Active strength
- 20 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 |
|---|
| 50090-7125-0 | 50090712500 | 30 TABLET in 1 BOTTLE (50090-7125-0) | 30 tablet | 2024-04-09 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Aripiprazole | A-S Medication Solutions | 2024-04-11 | HUMAN PRESCRIPTION DRUG LABEL | 1 |