Risperidone
- Product NDC
- 55111-208
- 11-digit product format
- 551110208
- Labeler code
- 55111
- Product ID
- 55111-208_9293825e-f154-ffc9-20b0-5846d813b7ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Risperidone
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Dr. Reddy's Laboratories Limited
- Application
- ANDA077328
- Marketing category
- ANDA
- Marketing start
- 2009-10-06
- 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 |
|---|
| 55111-208-78 | 55111020878 | 10 BLISTER PACK in 1 CARTON (55111-208-78) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 10 blister pack | 2009-10-06 | 0000-00-00 | No | No | Current |
| 55111-208-79 | 55111020879 | 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (55111-208-79) | | 2009-10-06 | 0000-00-00 | No | No | Current |
| 55111-208-81 | 55111020881 | 3 BLISTER PACK in 1 CARTON (55111-208-81) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 3 blister pack | 2009-10-06 | 0000-00-00 | No | No | Current |