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Serving hundreds of leading biopharmaceutical companies globally:

Chinese Patent Office
Express Scripts

Generated: March 21, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 072062

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NDA 072062 describes LOXAPINE SUCCINATE, which is a drug marketed by Elite Labs Inc, Lannett Holdings Inc, Mylan, and Watson Labs, and is included in seven NDAs. It is available from nine 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. Nine suppliers are listed for this compound. Additional details are available on the loxapine succinate profile page.
Summary for 072062
Applicant:Watson Labs
Ingredient:loxapine succinate
Therapeutic Class:Antipsychotics
Formulation / Manufacturing:see details
Suppliers and Packaging for NDA: 072062
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
LOXAPINE SUCCINATE loxapine succinate CAPSULE;ORAL 072062 ANDA Actavis Pharma, Inc. 0591-0372 N 0591-0372-01
LOXAPINE SUCCINATE loxapine succinate CAPSULE;ORAL 072062 ANDA REMEDYREPACK INC. 70518-0416 N 70518-0416-0

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:CAPSULE;ORALStrengthEQ 50MG BASE
Approval Date:Jun 15, 1988TE:ABRLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Chinese Patent Office
Boehringer Ingelheim
Federal Trade Commission

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