Risperidone
- Product NDC
- 63187-211
- 11-digit product format
- 631870211
- Labeler code
- 63187
- Product ID
- 63187-211_7f1960c6-8fd0-4dd5-9ff2-cf5478ea1445
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- risperidone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA078707
- Marketing category
- ANDA
- Marketing start
- 2008-12-29
- 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