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Serving leading biopharmaceutical companies globally:

Johnson and Johnson
Queensland Health
Mallinckrodt
Julphar
Novartis
Medtronic
AstraZeneca
Argus Health
Accenture
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Generated: January 21, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 072099

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NDA 072099 describes DESIPRAMINE HYDROCHLORIDE, which is a drug marketed by Actavis Totowa, Amneal Pharms Co, Ani Pharms Inc, Heritage Pharms Inc, Impax Labs Inc, Sandoz, 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 072099
Tradename:DESIPRAMINE HYDROCHLORIDE
Applicant:Sandoz
Ingredient:desipramine hydrochloride
Patents:0
Therapeutic Class:Antidepressants
Formulation / Manufacturing:see details
Pharmacology for NDA: 072099
Medical Subject Heading (MeSH) Categories for 072099
Suppliers and Packaging for NDA: 072099
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
DESIPRAMINE HYDROCHLORIDE desipramine hydrochloride TABLET;ORAL 072099 ANDA Sandoz Inc 0781-5218 0781-5218-10 1000 TABLET, FILM COATED in 1 BOTTLE (0781-5218-10)
DESIPRAMINE HYDROCHLORIDE desipramine hydrochloride TABLET;ORAL 072099 ANDA Sandoz Inc 0781-5218 0781-5218-01 100 TABLET, FILM COATED in 1 BOTTLE (0781-5218-01)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength10MG
Approval Date:May 24, 1988TE:ABRLD:No

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Serving leading biopharmaceutical companies globally:

Johnson and Johnson
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Federal Trade Commission
McKinsey
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