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Last Updated: March 18, 2024

Isoniazid - Generic Drug Details


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What are the generic sources for isoniazid and what is the scope of freedom to operate?

Isoniazid is the generic ingredient in eleven branded drugs marketed by Sandoz, Roche, Chartwell Rx, Cmp Pharma Inc, Lannett, Dow Pharm, Medpointe Pharm Hlc, Novartis, Barr, Duramed Pharms Barr, Epic Pharma Llc, Halsey, Hikma Intl Pharms, Impax Labs, Ivax Sub Teva Pharms, Lilly, Mk Labs, Nexgen Pharma Inc, Omnivium Pharms, Panray, Perrigo, Pharmavite, Phoenix Labs Ny, Purepac Pharm, Sun Pharm Industries, Thepharmanetwork Llc, Watson Labs, Whiteworth Town Plsn, Chartwell Molecular, Bristol Myers Squibb, Everylife, and Sanofi Aventis Us, and is included in forty-seven NDAs. Additional information is available in the individual branded drug profile pages.

There are five drug master file entries for isoniazid. Fourteen suppliers are listed for this compound.

Drug Prices for isoniazid

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Recent Clinical Trials for isoniazid

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SponsorPhase
University College, LondonPhase 2
Radboud University Medical CenterPhase 2
University of StellenboschPhase 2

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Pharmacology for isoniazid
Drug ClassAntimycobacterial
Medical Subject Heading (MeSH) Categories for isoniazid

US Patents and Regulatory Information for isoniazid

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Everylife STANOZIDE isoniazid TABLET;ORAL 080126-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Epic Pharma Llc ISONIAZID isoniazid TABLET;ORAL 008678-002 Approved Prior to Jan 1, 1982 DISCN Yes No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Chartwell Molecular LANIAZID isoniazid TABLET;ORAL 089776-001 Jun 13, 1988 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Impax Labs ISONIAZID isoniazid TABLET;ORAL 080153-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
>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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