Details for New Drug Application (NDA): 010775
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NDA 010775 describes TRILAFON, which is a drug marketed by Schering and is included in five NDAs. Additional details are available on the TRILAFON profile page.
The generic ingredient in TRILAFON is perphenazine. There are eight drug master file entries for this compound. Sixteen suppliers are listed for this compound. Additional details are available on the perphenazine profile page.
The generic ingredient in TRILAFON is perphenazine. There are eight drug master file entries for this compound. Sixteen suppliers are listed for this compound. Additional details are available on the perphenazine profile page.
Summary for 010775
| Tradename: | TRILAFON |
| Applicant: | Schering |
| Ingredient: | perphenazine |
| Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 010775
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | Yes | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | Yes | |||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | Yes | |||||
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