Risperidone
- Product NDC
- 63629-2283
- 11-digit product format
- 636292283
- Labeler code
- 63629
- Product ID
- 63629-2283_0ec2666e-b6cd-4803-ba42-3e37ffed8ab7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Risperidone
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077494
- Marketing category
- ANDA
- Marketing start
- 2009-06-01
- Marketing end
- 0000-00-00
- Substance
- RISPERIDONE
- Active strength
- 0 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2283-1 | 63629228301 | 5 BLISTER PACK in 1 CARTON (63629-2283-1) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 5 blister pack | 2021-05-19 | 0000-00-00 | No | No | Current |