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Generated: August 21, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 072101

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NDA 072101 describes DESIPRAMINE HYDROCHLORIDE, which is a drug marketed by Sandoz, Actavis Totowa, Ani Pharms Inc, Amneal Pharms Co, Heritage Pharms Inc, Impax Labs Inc, and Usl Pharma, and is included in nineteen NDAs. It is available from thirteen suppliers. Additional details are available on the DESIPRAMINE HYDROCHLORIDE profile page.

The generic ingredient in DESIPRAMINE HYDROCHLORIDE is desipramine hydrochloride. There are nine drug master file entries for this compound. Sixteen suppliers are listed for this compound. Additional details are available on the desipramine hydrochloride profile page.

Summary for NDA: 072101

Tradename:
1
Applicant:
1
Ingredient:
1
Patents:0
Therapeutic Class:Antidepressants
Formulation / Manufacturing:see details

Pharmacology for NDA: 072101

Suppliers and Packaging for NDA: 072101

Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
DESIPRAMINE HYDROCHLORIDE
desipramine hydrochloride
TABLET;ORAL 072101 ANDA Sandoz Inc 0781-1973 0781-1973-01 100 TABLET, FILM COATED in 1 BOTTLE (0781-1973-01)
DESIPRAMINE HYDROCHLORIDE
desipramine hydrochloride
TABLET;ORAL 072101 ANDA Sandoz Inc 0781-1973 0781-1973-10 1000 TABLET, FILM COATED in 1 BOTTLE (0781-1973-10)

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength50MG
Approval Date:May 24, 1988TE:ABRLD:No


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