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Last Updated: October 5, 2024

PRAVASTATIN Drug Patent Profile


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Which patents cover Pravastatin, and what generic alternatives are available?

Pravastatin is a drug marketed by Accord Hlthcare, Apnar Pharma Lp, Apotex, Aurobindo Pharma, Biocon Pharma, Chartwell Rx, Cipla, Dr Reddys Labs Inc, Glenmark Pharms Ltd, Hisun Pharm Hangzhou, Norvium Bioscience, Pliva Hrvatska Doo, Ranbaxy Labs Ltd, Teva, Teva Pharms, Watson Labs, and Zydus Pharms Usa. and is included in eighteen NDAs.

The generic ingredient in PRAVASTATIN is pravastatin sodium. There are sixteen drug master file entries for this compound. Forty suppliers are listed for this compound. Additional details are available on the pravastatin sodium profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Pravastatin

A generic version of PRAVASTATIN was approved as pravastatin sodium by TEVA on April 24th, 2006.

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Drug patent expirations by year for PRAVASTATIN
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US Patents and Regulatory Information for PRAVASTATIN

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Norvium Bioscience PRAVASTATIN SODIUM pravastatin sodium TABLET;ORAL 079187-001 May 27, 2010 DISCN No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Dr Reddys Labs Inc PRAVASTATIN SODIUM pravastatin sodium TABLET;ORAL 076714-004 Dec 28, 2007 AB RX No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Pliva Hrvatska Doo PRAVASTATIN SODIUM pravastatin sodium TABLET;ORAL 077730-002 Nov 21, 2006 DISCN No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Watson Labs PRAVASTATIN SODIUM pravastatin sodium TABLET;ORAL 076939-004 Oct 23, 2006 AB RX No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Norvium Bioscience PRAVASTATIN SODIUM pravastatin sodium TABLET;ORAL 079187-003 May 27, 2010 DISCN No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Pliva Hrvatska Doo PRAVASTATIN SODIUM pravastatin sodium TABLET;ORAL 077730-003 Nov 21, 2006 DISCN No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

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