Aripiprazole
- Product NDC
- 43353-140
- 11-digit product format
- 433530140
- Labeler code
- 43353
- Product ID
- 43353-140_d4065c9f-d681-4d49-af2b-a12985ca3e57
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA078583
- Marketing category
- ANDA
- Marketing start
- 2015-07-28
- Marketing end
- 0000-00-00
- Substance
- ARIPIPRAZOLE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 43353-140-15 | 43353014015 | 15 TABLET in 1 BOTTLE (43353-140-15) | 15 tablet | 2016-02-15 | 0000-00-00 | No | No | Current |
| 43353-140-45 | 43353014045 | 45 TABLET in 1 BOTTLE (43353-140-45) | 45 tablet | 2016-02-15 | 0000-00-00 | No | No | Current |