Aripiprazole
- Product NDC
- 16714-787
- 11-digit product format
- 167140787
- Labeler code
- 16714
- Product ID
- 16714-787_7cc1f9b2-79b0-45d9-8559-834df504f5ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NorthStar RxLLC
- Application
- ANDA204111
- Marketing category
- ANDA
- Marketing start
- 2018-03-07
- Marketing end
- 0000-00-00
- Substance
- ARIPIPRAZOLE
- Active strength
- 20 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 |
|---|
| 16714-787-01 | 16714078701 | 30 TABLET in 1 BOTTLE (16714-787-01) | 30 tablet | 2018-03-07 | 0000-00-00 | No | No | Current |