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Last Updated: December 7, 2021

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 205232


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NDA 205232 describes PERPHENAZINE, which is a drug marketed by Pharm Assoc, Ani Pharms, Mylan, Rising, Sandoz, Vintage Pharms, Watson Labs Inc, Wilshire Pharms Inc, Zydus Pharms, Fosun Pharma, Heritage Pharma, Ivax Sub Teva Pharms, Par Pharm, Sun Pharm Industries, and Watson Labs, and is included in forty-seven NDAs. It is available from thirteen 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 205232
Tradename:PERPHENAZINE
Applicant:Zydus Pharms
Ingredient:perphenazine
Patents:0
Formulation / Manufacturing:see details
Pharmacology for NDA: 205232
Medical Subject Heading (MeSH) Categories for 205232
Suppliers and Packaging for NDA: 205232
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
PERPHENAZINE perphenazine TABLET;ORAL 205232 ANDA Zydus Pharmaceuticals (USA) Inc. 68382-591 68382-591-01 100 TABLET in 1 BOTTLE (68382-591-01)
PERPHENAZINE perphenazine TABLET;ORAL 205232 ANDA Zydus Pharmaceuticals (USA) Inc. 68382-591 68382-591-05 500 TABLET in 1 BOTTLE (68382-591-05)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength2MG
Approval Date:Apr 6, 2020TE:ABRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength4MG
Approval Date:Apr 6, 2020TE:ABRLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength8MG
Approval Date:Apr 6, 2020TE:ABRLD:No

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