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Last Updated: April 24, 2024

Methacholine chloride - Generic Drug Details

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What are the generic sources for methacholine chloride and what is the scope of patent protection?

Methacholine chloride is the generic ingredient in one branded drug marketed by Methapharm and is included in one NDA. Additional information is available in the individual branded drug profile pages.

There is one drug master file entry for methacholine chloride. One supplier is listed for this compound.

Summary for methacholine chloride

US Patents:	0
Tradenames:	1
Applicants:	1
NDAs:	1
Drug Master File Entries:	1
Finished Product Suppliers / Packagers:	1
Raw Ingredient (Bulk) Api Vendors:	79
Clinical Trials:	12
Patent Applications:	5,922
Formulation / Manufacturing:	see details
What excipients (inactive ingredients) are in methacholine chloride?	methacholine chloride excipients list
DailyMed Link:	methacholine chloride at DailyMed

Recent Clinical Trials for methacholine chloride

Identify potential brand extensions & 505(b)(2) entrants

Sponsor	Phase
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.	N/A
Aurobindo Pharma Ltd	Phase 3
University of Saskatchewan	Phase 4

See all methacholine chloride clinical trials

Pharmacology for methacholine chloride

Drug Class	Cholinergic Receptor Agonist
Mechanism of Action	Cholinergic Agonists

Medical Subject Heading (MeSH) Categories for methacholine chloride

Bronchoconstrictor Agents
Miotics
Muscarinic Agonists
Parasympathomimetics

US Patents and Regulatory Information for methacholine chloride

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Glossary

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	TE	Type	RLD	RS	Patent No.	Patent Expiration	Product	Substance	Delist Req.	Exclusivity Expiration
Methapharm	PROVOCHOLINE	methacholine chloride	FOR SOLUTION;INHALATION	019193-002	Aug 29, 2016		DISCN	Yes	No	⤷ Try a Trial	⤷ Try a Trial				⤷ Try a Trial
Methapharm	PROVOCHOLINE	methacholine chloride	FOR SOLUTION;INHALATION	019193-001	Oct 31, 1986		RX	Yes	Yes	⤷ 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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