Latuda
- Product NDC
- 70518-1936
- 11-digit product format
- 705181936
- Labeler code
- 70518
- Product ID
- 70518-1936_ba9db2b8-c058-59ce-e053-2995a90a2971
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lurasidone hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA200603
- Marketing category
- NDA
- Marketing start
- 2019-03-06
- Marketing end
- 0000-00-00
- Substance
- LURASIDONE HYDROCHLORIDE
- Active strength
- 120 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 |
|---|
| 70518-1936-0 | 70518193600 | 30 POUCH in 1 BOX, UNIT-DOSE (70518-1936-0) > 1 TABLET, FILM COATED in 1 POUCH (70518-1936-1) | 30 pouch | 2019-03-06 | 0000-00-00 | No | No | Current |