Aripiprazole
- Product NDC
- 70518-2471
- 11-digit product format
- 705182471
- Labeler code
- 70518
- Product ID
- 70518-2471_993c0fc9-919e-1dbd-e053-2995a90a1a6a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204111
- Marketing category
- ANDA
- Marketing start
- 2019-12-06
- 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