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Details for New Drug Application (NDA): 072062

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NDA 072062 describes LOXAPINE SUCCINATE, which is a drug marketed by Watson Labs, Mylan, Elite Labs Inc, and Lannett Holdings Inc, and is included in seven NDAs. It is available from ten 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. Ten suppliers are listed for this compound. Additional details are available on the loxapine succinate profile page.

Summary for NDA: 072062

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
CAPSULE;ORAL 072062 ANDA Actavis Pharma, Inc. 0591-0372 0591-0372-01 100 CAPSULE in 1 BOTTLE, PLASTIC (0591-0372-01)
loxapine succinate
CAPSULE;ORAL 072062 ANDA Clinical Solutions Wholesale 58118-0372 58118-0372-0 1 CAPSULE in 1 PACKAGE (58118-0372-0)

Summary for product number 001

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

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