aripiprazole
- Product NDC
- 0904-6655
- 11-digit product format
- 009046655
- Labeler code
- 0904
- Product ID
- 0904-6655_a98b93f6-0fca-441d-9ed6-4a5c5618a6ad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA201519
- Marketing category
- ANDA
- Marketing start
- 2015-04-28
- Marketing end
- 0000-00-00
- Substance
- ARIPIPRAZOLE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record