Aripiprazole
- Product NDC
- 70518-1421
- 11-digit product format
- 705181421
- Labeler code
- 70518
- Product ID
- 70518-1421_e41a1893-01b8-3fd4-e053-2a95a90a13ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204838
- Marketing category
- ANDA
- Marketing start
- 2018-09-18
- Marketing end
- 0000-00-00
- Substance
- ARIPIPRAZOLE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1421-0 | 70518142100 | 28 TABLET in 1 BLISTER PACK (70518-1421-0) | 28 tablet | 2018-09-18 | 0000-00-00 | No | No | Current |
| 70518-1421-1 | 70518142101 | 30 POUCH in 1 BOX (70518-1421-1) > 1 TABLET in 1 POUCH (70518-1421-2) | 30 pouch | 2019-04-23 | 0000-00-00 | No | No | Current |
| 70518-1421-3 | 70518142103 | 30 TABLET in 1 BLISTER PACK (70518-1421-3) | 30 tablet | 2021-08-10 | 0000-00-00 | No | No | Current |