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Latuda
Latuda - 63402-308-50 - (lurasidone hydrochloride)
Drug Information of Latuda
| Product NDC: | 63402-308 |
| Proprietary Name: | Latuda |
| Non Proprietary Name: | lurasidone hydrochloride |
| Active Ingredient(s): | 80 mg/1 & nbsp; lurasidone hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Latuda
| Product NDC: | 63402-308 |
| Labeler Name: | Sunovion Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA200603 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20101028 |
Package Information of Latuda
| Package NDC: | 63402-308-50 |
| Package Description: | 500 TABLET, FILM COATED in 1 BOTTLE (63402-308-50) |
NDC Information of Latuda
| NDC Code | 63402-308-50 |
| Proprietary Name | Latuda |
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (63402-308-50) |
| Product NDC | 63402-308 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lurasidone hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20101028 |
| Marketing Category Name | NDA |
| Labeler Name | Sunovion Pharmaceuticals Inc. |
| Substance Name | LURASIDONE HYDROCHLORIDE |
| Strength Number | 80 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
