Aripiprazole
- Product NDC
- 70518-1859
- 11-digit product format
- 705181859
- Labeler code
- 70518
- Product ID
- 70518-1859_9696aefb-c9ae-d959-e053-2a95a90ad531
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA206174
- Marketing category
- ANDA
- Marketing start
- 2019-02-07
- 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