RISPERIDONE
- Product NDC
- 63629-8121
- 11-digit product format
- 636298121
- Labeler code
- 63629
- Product ID
- 63629-8121_8ee00a01-c80f-4fc4-bf59-d27d85ae4e08
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- RISPERIDONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA201003
- Marketing category
- ANDA
- Marketing start
- 2014-03-28
- Marketing end
- 0000-00-00
- Substance
- RISPERIDONE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 63629-8121-1 | 63629812101 | 30 TABLET in 1 BOTTLE (63629-8121-1) | 30 tablet | 2019-07-25 | 0000-00-00 | No | No | Current |