Aripiprazole
- Product NDC
- 13811-683
- 11-digit product format
- 138110683
- Labeler code
- 13811
- Product ID
- 13811-683_f07ffa73-6b9b-44fe-873f-88aba0bf2325
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Trigen Laboratories, LLC
- Application
- ANDA202101
- Marketing category
- ANDA
- Marketing start
- 2015-04-28
- Marketing end
- 0000-00-00
- Substance
- ARIPIPRAZOLE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record