RISPERIDONE
- Product NDC
- 68788-7211
- 11-digit product format
- 687887211
- Labeler code
- 68788
- Product ID
- 68788-7211_1376c8b1-0636-4a96-8952-afd2b3a48c7c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- RISPERIDONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA201003
- Marketing category
- ANDA
- Marketing start
- 2018-08-06
- Marketing end
- 0000-00-00
- Substance
- RISPERIDONE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7211-3 | 68788721103 | 30 TABLET in 1 BOTTLE (68788-7211-3) | 30 tablet | 2018-08-06 | 0000-00-00 | No | No | Current |
| 68788-7211-6 | 68788721106 | 60 TABLET in 1 BOTTLE (68788-7211-6) | 60 tablet | 2018-08-06 | 0000-00-00 | No | No | Current |
| 68788-7211-9 | 68788721109 | 90 TABLET in 1 BOTTLE (68788-7211-9) | 90 tablet | 2018-08-06 | 0000-00-00 | No | No | Current |