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Last Updated: December 22, 2024

Details for New Drug Application (NDA): 216542

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NDA 216542 describes NEOSTIGMINE METHYLSULFATE, which is a drug marketed by Adaptis, Am Regent, Amneal, Amphastar Pharms Inc, Amring Pharms, Be Pharms, Caplin, Dr Reddys, Endo Operations, Eugia Pharma, Fresenius Kabi Usa, Gland Pharma Ltd, Hikma, Meitheal, Sagent Pharms Inc, and Umedica, and is included in eighteen NDAs. It is available from twenty-three suppliers. Additional details are available on the NEOSTIGMINE METHYLSULFATE profile page.

The generic ingredient in NEOSTIGMINE METHYLSULFATE is neostigmine methylsulfate. There are nine drug master file entries for this compound. Twenty-five suppliers are listed for this compound. Additional details are available on the neostigmine methylsulfate profile page.

Summary for 216542

Tradename:	NEOSTIGMINE METHYLSULFATE
Applicant:	Sagent Pharms Inc
Ingredient:	neostigmine methylsulfate
Patents:	0

Medical Subject Heading (MeSH) Categories for 216542

Cholinesterase Inhibitors
Parasympathomimetics

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	SOLUTION;INTRAVENOUS			Strength	5MG/10ML (0.5MG/ML)
Approval Date:	Feb 17, 2023	TE:	AP	RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	SOLUTION;INTRAVENOUS			Strength	10MG/10ML (1MG/ML)
Approval Date:	Feb 17, 2023	TE:	AP	RLD:	No

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