Risperidone
- Product NDC
- 71335-2645
- 11-digit product format
- 713352645
- Labeler code
- 71335
- Product ID
- 71335-2645_e568a5f6-8644-497b-9893-f84bd2486225
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Risperidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077493
- Marketing category
- ANDA
- Marketing start
- 2014-06-01
- Substance
- RISPERIDONE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| L6UH7ZF8HC | RISPERIDONE | 106266-06-2 | RISPERIDONE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2645-1 | 71335264501 | 60 TABLET in 1 BOTTLE (71335-2645-1) | 60 tablet | 2025-06-03 | No | No | Historical |
| 71335-2645-2 | 71335264502 | 30 TABLET in 1 BOTTLE (71335-2645-2) | 30 tablet | 2025-06-03 | No | No | Historical |
| 71335-2645-3 | 71335264503 | 90 TABLET in 1 BOTTLE (71335-2645-3) | 90 tablet | 2025-06-03 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Risperidone | Bryant Ranch Prepack | 2025-06-03 | HUMAN PRESCRIPTION DRUG LABEL | 1 |