aripiprazole
- Product NDC
- 68788-7006
- 11-digit product format
- 687887006
- Labeler code
- 68788
- Product ID
- 68788-7006_bd2ef8df-4b43-4151-9f23-c82a0a829daf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA201519
- Marketing category
- ANDA
- Marketing start
- 2017-08-16
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7006-1 | 68788700601 | 100 TABLET in 1 BOTTLE (68788-7006-1) | 100 tablet | 2017-08-16 | 0000-00-00 | No | No | Current |
| 68788-7006-2 | 68788700602 | 20 TABLET in 1 BOTTLE (68788-7006-2) | 20 tablet | 2017-08-16 | 0000-00-00 | No | No | Current |
| 68788-7006-3 | 68788700603 | 30 TABLET in 1 BOTTLE (68788-7006-3) | 30 tablet | 2017-08-16 | 0000-00-00 | No | No | Current |
| 68788-7006-6 | 68788700606 | 60 TABLET in 1 CARTON (68788-7006-6) | 60 tablet | 2017-08-16 | 0000-00-00 | No | No | Current |
| 68788-7006-9 | 68788700609 | 90 TABLET in 1 BOTTLE (68788-7006-9) | 90 tablet | 2017-08-16 | 0000-00-00 | No | No | Current |