Details for New Drug Application (NDA): 018580

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NDA 018580 describes YUTOPAR, which is a drug marketed by Astrazeneca and is included in two NDAs. Additional details are available on the YUTOPAR profile page.

The generic ingredient in YUTOPAR is ritodrine hydrochloride. There are five drug master file entries for this compound. Additional details are available on the ritodrine hydrochloride profile page.

Summary for 018580

Tradename:	YUTOPAR
Applicant:	Astrazeneca
Ingredient:	ritodrine hydrochloride
Patents:	0

Medical Subject Heading (MeSH) Categories for 018580

Adrenergic beta-2 Receptor Agonists
Sympathomimetics
Tocolytic Agents

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	INJECTABLE;INJECTION			Strength	10MG/ML
Approval Date:	Approved Prior to Jan 1, 1982	TE:		RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	DISCN	Dosage:	INJECTABLE;INJECTION			Strength	15MG/ML
Approval Date:	Sep 27, 1984	TE:		RLD:	No

Expired US Patents for NDA 018580

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Astrazeneca	YUTOPAR	ritodrine hydrochloride	INJECTABLE;INJECTION	018580-001	Approved Prior to Jan 1, 1982	⤷ Subscribe	⤷ Subscribe
Astrazeneca	YUTOPAR	ritodrine hydrochloride	INJECTABLE;INJECTION	018580-002	Sep 27, 1984	⤷ Subscribe	⤷ Subscribe
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

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