aripiprazole
- Product NDC
- 63629-7017
- 11-digit product format
- 636297017
- Labeler code
- 63629
- Product ID
- 63629-7017_54a06923-241b-46fc-b8cf-155d227ae691
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA201519
- Marketing category
- ANDA
- Marketing start
- 2015-04-28
- Marketing end
- 0000-00-00
- Substance
- ARIPIPRAZOLE
- Active strength
- 2 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 |
|---|
| 63629-7017-1 | 63629701701 | 30 TABLET in 1 BOTTLE (63629-7017-1) | 30 tablet | 2016-05-26 | 0000-00-00 | No | No | Current |
| 63629-7017-2 | 63629701702 | 28 TABLET in 1 BOTTLE (63629-7017-2) | 28 tablet | 2022-04-29 | 0000-00-00 | No | No | Current |
| 63629-7017-3 | 63629701703 | 90 TABLET in 1 BOTTLE (63629-7017-3) | 90 tablet | 2018-09-05 | 0000-00-00 | No | No | Current |
| 63629-7017-4 | 63629701704 | 60 TABLET in 1 BOTTLE (63629-7017-4) | 60 tablet | 2022-04-29 | 0000-00-00 | No | No | Current |