Details for New Drug Application (NDA): 076762
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NDA 076762 describes LOXAPINE SUCCINATE, which is a drug marketed by Elite Labs Inc, Lannett Co Inc, Rising, and Watson Labs, and is included in seven NDAs. It is available from six suppliers. Additional details are available on the LOXAPINE SUCCINATE profile page.
The generic ingredient in LOXAPINE SUCCINATE is loxapine succinate. There are eight drug master file entries for this compound. Six suppliers are listed for this compound. Additional details are available on the loxapine succinate profile page.
The generic ingredient in LOXAPINE SUCCINATE is loxapine succinate. There are eight drug master file entries for this compound. Six suppliers are listed for this compound. Additional details are available on the loxapine succinate profile page.
Summary for 076762
| Tradename: | LOXAPINE SUCCINATE |
| Applicant: | Rising |
| Ingredient: | loxapine succinate |
| Patents: | 0 |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE;ORAL | Strength | EQ 5MG BASE | ||||
| Approval Date: | Nov 1, 2004 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE;ORAL | Strength | EQ 10MG BASE | ||||
| Approval Date: | Nov 1, 2004 | TE: | RLD: | No | |||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE;ORAL | Strength | EQ 25MG BASE | ||||
| Approval Date: | Nov 1, 2004 | TE: | RLD: | No | |||||
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