FdaApplication
NDA 000793
Identifiers
- fda_app_no: NDA000793
Properties
| Property | Value |
|---|---|
| applicant_name | PHARMOBEDIENT CONSULTING LLC |
| application_type | NDA |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BUTISOL SODIUM | BUTABARBITAL SODIUM | 30MG | TABLET;ORAL |
| BUTISOL SODIUM | BUTABARBITAL SODIUM | 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| BUTISOL SODIUM | BUTABARBITAL SODIUM | 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| BUTISOL SODIUM | BUTABARBITAL SODIUM | 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
4 products