Risperidone
- Product NDC
- 0781-5312
- 11-digit product format
- 007815312
- Labeler code
- 0781
- Product ID
- 0781-5312_483b5267-344e-4ba9-b6d8-a8bff8f7108e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Risperidone
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA078116
- Marketing category
- ANDA
- Marketing start
- 2009-12-22
- Marketing end
- 0000-00-00
- Substance
- RISPERIDONE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 0781-5312-08 | 00781531208 | 28 BLISTER PACK in 1 CARTON (0781-5312-08) > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0781-5312-06) | 28 blister pack | 2009-12-22 | 0000-00-00 | No | No | Current |