risperidone
- Product NDC
- 55700-082
- 11-digit product format
- 557000082
- Labeler code
- 55700
- Product ID
- 55700-082_49e9ce05-c620-47bb-af07-6567acfc9f60
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- risperidone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA078040
- Marketing category
- ANDA
- Marketing start
- 2014-01-10
- Marketing end
- 0000-00-00
- Substance
- RISPERIDONE
- Active strength
- 0 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-082-60 | 55700008260 | 60 TABLET, FILM COATED in 1 BOTTLE (55700-082-60) | 2014-01-10 | 0000-00-00 | No | No | Current |