Aripiprazole
- Product NDC
- 70518-2567
- 11-digit product format
- 705182567
- Labeler code
- 70518
- Product ID
- 70518-2567_d6a947f6-0037-2dd3-e053-2995a90a30ab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204838
- Marketing category
- ANDA
- Marketing start
- 2020-02-05
- Marketing end
- 0000-00-00
- Substance
- ARIPIPRAZOLE
- Active strength
- 15 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2567-0 | 70518256700 | 30 POUCH in 1 BOX (70518-2567-0) > 1 TABLET in 1 POUCH (70518-2567-1) | 30 pouch | 2020-02-05 | 0000-00-00 | No | No | Current |