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Last Updated: March 18, 2024

CIMETIDINE Drug Patent Profile


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When do Cimetidine patents expire, and what generic alternatives are available?

Cimetidine is a drug marketed by Apotex, Chartwell Molecules, Chartwell Rx, Contract Pharmacal, Cycle, Hikma, Ivax Sub Teva Pharms, L Perrigo Co, Mylan, Novitium Pharma, Perrigo, Pliva, Sandoz, Teva, Upsher Smith Labs, Watson Labs Inc, Watson Labs Teva, Dava Pharms Inc, Hospira, Luitpold, Teva Parenteral, Vintage Pharms Llc, Ani Pharms, Chartwell Molecular, G And W Labs Inc, Pai Holdings Pharm, Pharm Assoc, and Pharmobedient Cnsltg. and is included in forty-nine NDAs.

The generic ingredient in CIMETIDINE is cimetidine hydrochloride. There are twenty-five drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the cimetidine hydrochloride profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Cimetidine

A generic version of CIMETIDINE was approved as cimetidine hydrochloride by PHARM ASSOC on January 27th, 1997.

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Drug patent expirations by year for CIMETIDINE
Drug Prices for CIMETIDINE

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Recent Clinical Trials for CIMETIDINE

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SponsorPhase
Assiut UniversityEarly Phase 1
Peking UniversityPhase 2
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.Phase 2

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Pharmacology for CIMETIDINE
Medical Subject Heading (MeSH) Categories for CIMETIDINE

US Patents and Regulatory Information for CIMETIDINE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Teva Parenteral CIMETIDINE HYDROCHLORIDE cimetidine hydrochloride INJECTABLE;INJECTION 074252-001 Nov 26, 1997 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Pliva CIMETIDINE cimetidine TABLET;ORAL 074566-001 Feb 27, 1997 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Mylan CIMETIDINE cimetidine TABLET;ORAL 074246-003 May 17, 1994 AB RX 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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