RISPERIDONE
- Product NDC
- 68071-3356
- 11-digit product format
- 680713356
- Labeler code
- 68071
- Product ID
- 68071-3356_548a84fc-7716-673b-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- RISPERIDONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Nucare Pharmaceuticals,Inc.
- Application
- ANDA201003
- Marketing category
- ANDA
- Marketing start
- 2014-03-28
- Marketing end
- 0000-00-00
- Substance
- RISPERIDONE
- 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