Aripiprazole
- Product NDC
- 70518-0683
- 11-digit product format
- 705180683
- Labeler code
- 70518
- Product ID
- 70518-0683_8ac1e728-fb64-3350-e053-2a95a90aad3a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA205064
- Marketing category
- ANDA
- Marketing start
- 2017-08-16
- Marketing end
- 0000-00-00
- Substance
- ARIPIPRAZOLE
- Active strength
- 15 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record