Make Better Decisions - Finding and Evaluating Generic and Branded Drug Market Entry Opportunities

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Finding and Evaluating Generic and Branded Drug Market Entry Opportunities

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Last Updated: December 12, 2019

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 089685

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NDA 089685 describes PERPHENAZINE, which is a drug marketed by Pharm Assoc, Anda Repository, Ani Pharms Inc, Mylan, Sandoz, Vintage Pharms, Watson Labs Inc, Wilshire Pharms Inc, Fosun Pharma, Heritage Pharma, Ivax Sub Teva Pharms, Par Pharm, Sun Pharm Industries, and Watson Labs, and is included in forty-six NDAs. It is available from twelve suppliers. Additional details are available on the PERPHENAZINE profile page.

The generic ingredient in PERPHENAZINE is amitriptyline hydrochloride; perphenazine. There are thirteen drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the amitriptyline hydrochloride; perphenazine profile page.
Summary for 089685
Tradename:PERPHENAZINE
Applicant:Sandoz
Ingredient:perphenazine
Patents:0
Formulation / Manufacturing:see details
Pharmacology for NDA: 089685
Medical Subject Heading (MeSH) Categories for 089685
Suppliers and Packaging for NDA: 089685
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
PERPHENAZINE perphenazine TABLET;ORAL 089685 ANDA Sandoz Inc 0781-1046 0781-1046-01 100 TABLET, FILM COATED in 1 BOTTLE (0781-1046-01)
PERPHENAZINE perphenazine TABLET;ORAL 089685 ANDA Sandoz Inc 0781-1046 0781-1046-10 1000 TABLET, FILM COATED in 1 BOTTLE (0781-1046-10)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength8MG
Approval Date:Dec 8, 1988TE:ABRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength2MG
Approval Date:Dec 8, 1988TE:ABRLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength4MG
Approval Date:Dec 8, 1988TE:ABRLD:No

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