Risperidone
- Product NDC
- 0904-6362
- 11-digit product format
- 009046362
- Labeler code
- 0904
- Product ID
- 0904-6362_f68fdc24-2093-4ac8-9a03-5f03f5bf0b8a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Risperidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA079088
- Marketing category
- ANDA
- Marketing start
- 2013-11-30
- Marketing end
- 0000-00-00
- Substance
- RISPERIDONE
- Active strength
- 4 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 |
|---|
| 0904-6362-61 | 00904636261 | 100 TABLET in 1 BOX, UNIT-DOSE (0904-6362-61) | 100 tablet | 2013-11-30 | 0000-00-00 | No | No | Current |