Aripiprazole
- Product NDC
- 70518-2514
- 11-digit product format
- 705182514
- Labeler code
- 70518
- Product ID
- 70518-2514_ba4d4d38-d4aa-1013-e053-2a95a90ab9fe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204838
- Marketing category
- ANDA
- Marketing start
- 2019-12-31
- Marketing end
- 0000-00-00
- Substance
- ARIPIPRAZOLE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 70518-2514-0 | 70518251400 | 30 POUCH in 1 BOX (70518-2514-0) > 1 TABLET in 1 POUCH (70518-2514-1) | 30 pouch | 2019-12-31 | 0000-00-00 | No | No | Current |
| 70518-2514-2 | 70518251402 | 30 TABLET in 1 BLISTER PACK (70518-2514-2) | 30 tablet | 2021-01-30 | 0000-00-00 | No | No | Current |