aripiprazole
- Product NDC
- 70934-001
- 11-digit product format
- 709340001
- Labeler code
- 70934
- Product ID
- 70934-001_78476279-5af3-2301-e053-2a91aa0ab186
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA201519
- Marketing category
- ANDA
- Marketing start
- 2017-02-21
- 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