Aripiprazole
- Product NDC
- 70518-1144
- 11-digit product format
- 705181144
- Labeler code
- 70518
- Product ID
- 70518-1144_90751991-8e51-7f1e-e053-2a95a90a0696
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078607
- Marketing category
- ANDA
- Marketing start
- 2018-04-27
- Marketing end
- 0000-00-00
- Substance
- ARIPIPRAZOLE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record