RISPERIDONE
- Product NDC
- 55700-392
- 11-digit product format
- 557000392
- Labeler code
- 55700
- Product ID
- 55700-392_880d4c39-8349-466e-9b18-205956aa3224
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- RISPERIDONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA201003
- Marketing category
- ANDA
- Marketing start
- 2015-09-09
- Marketing end
- 0000-00-00
- Substance
- RISPERIDONE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record