Risperidone
- Product NDC
- 65862-119
- 11-digit product format
- 658620119
- Labeler code
- 65862
- Product ID
- 65862-119_5d2750a4-025a-40a1-97d2-d9447a37afbb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Risperidone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA078269
- Marketing category
- ANDA
- Marketing start
- 2008-10-08
- Marketing end
- 0000-00-00
- Substance
- RISPERIDONE
- Active strength
- 0 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record