Details for New Drug Application (NDA): 018733

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NDA 018733 describes TALWIN NX, which is a drug marketed by Sanofi Aventis Us and is included in one NDA. Additional details are available on the TALWIN NX profile page.

The generic ingredient in TALWIN NX is naloxone hydrochloride; pentazocine hydrochloride. There are twelve drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the naloxone hydrochloride; pentazocine hydrochloride profile page.

Summary for 018733

Tradename:	TALWIN NX
Applicant:	Sanofi Aventis Us
Ingredient:	naloxone hydrochloride; pentazocine hydrochloride
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	EQ 0.5MG BASE;EQ 50MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons
Approval Date:	Dec 16, 1982	TE:		RLD:	No

Expired US Patents for NDA 018733

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Sanofi Aventis Us	TALWIN NX	naloxone hydrochloride; pentazocine hydrochloride	TABLET;ORAL	018733-001	Dec 16, 1982	⤷ Sign Up	⤷ Sign Up
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

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