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Last Updated: April 19, 2024

Details for New Drug Application (NDA): 020872

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NDA 020872 describes CHILDREN'S ALLEGRA HIVES, which is a drug marketed by Chattem Sanofi and is included in three NDAs. It is available from four suppliers. There is one patent protecting this drug. Additional details are available on the CHILDREN'S ALLEGRA HIVES profile page.

The generic ingredient in CHILDREN'S ALLEGRA HIVES is fexofenadine hydrochloride. There are twenty-three drug master file entries for this compound. One hundred and one suppliers are listed for this compound. Additional details are available on the fexofenadine hydrochloride profile page.

Summary for 020872

Tradename:	CHILDREN'S ALLEGRA HIVES
Applicant:	Chattem Sanofi
Ingredient:	fexofenadine hydrochloride
Patents:	0
Formulation / Manufacturing:	see details

Pharmacology for NDA: 020872

Mechanism of Action	Histamine H1 Receptor Antagonists

Suppliers and Packaging for NDA: 020872

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
ALLEGRA ALLERGY	fexofenadine hydrochloride	TABLET;ORAL	020872	NDA	Chattem, Inc.	41167-4120	41167-4120-0	1 BLISTER PACK in 1 CARTON (41167-4120-0) / 5 TABLET, FILM COATED in 1 BLISTER PACK
ALLEGRA ALLERGY	fexofenadine hydrochloride	TABLET;ORAL	020872	NDA	Chattem, Inc.	41167-4120	41167-4120-1	1 BLISTER PACK in 1 CARTON (41167-4120-1) / 2 TABLET, FILM COATED in 1 BLISTER PACK

Profile for product number 005

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	30MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons
Approval Date:	Jan 24, 2011	TE:		RLD:	Yes

Profile for product number 006

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	30MG
Approval Date:	Jan 24, 2011	TE:		RLD:	Yes

Profile for product number 007

Active Rx/OTC/Discontinued:	OTC	Dosage:	TABLET;ORAL			Strength	60MG
Approval Date:	Jan 24, 2011	TE:		RLD:	Yes

Expired US Patents for NDA 020872

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Chattem Sanofi	CHILDREN'S ALLEGRA HIVES	fexofenadine hydrochloride	TABLET;ORAL	020872-006	Jan 24, 2011	⤷ Try a Trial	⤷ Try a Trial
Chattem Sanofi	ALLEGRA ALLERGY	fexofenadine hydrochloride	TABLET;ORAL	020872-007	Jan 24, 2011	⤷ Try a Trial	⤷ Try a Trial
Chattem Sanofi	CHILDREN'S ALLEGRA HIVES	fexofenadine hydrochloride	TABLET;ORAL	020872-006	Jan 24, 2011	⤷ Try a Trial	⤷ Try a Trial
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.