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Generated: December 14, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 020468

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NDA 020468 describes NASACORT ALLERGY 24 HOUR, which is a drug marketed by Sanofi Aventis Us and is included in one NDA. It is available from two suppliers. Additional details are available on the NASACORT ALLERGY 24 HOUR profile page.

The generic ingredient in NASACORT ALLERGY 24 HOUR is triamcinolone acetonide. There are fifty-one drug master file entries for this compound. Eighty-two suppliers are listed for this compound. Additional details are available on the triamcinolone acetonide profile page.
Summary for 020468
Tradename:NASACORT ALLERGY 24 HOUR
Applicant:Sanofi Aventis Us
Ingredient:triamcinolone acetonide
Patents:0
Formulation / Manufacturing:see details
Medical Subject Heading (MeSH) Categories for 020468
Suppliers and Packaging for NDA: 020468
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
NASACORT ALLERGY 24 HOUR triamcinolone acetonide SPRAY, METERED;NASAL 020468 NDA Chattem, Inc. 41167-5800 41167-5800-1 1 BOTTLE, SPRAY in 1 CARTON (41167-5800-1) > 30 SPRAY, METERED in 1 BOTTLE, SPRAY
NASACORT ALLERGY 24 HOUR triamcinolone acetonide SPRAY, METERED;NASAL 020468 NDA Chattem, Inc. 41167-5800 41167-5800-2 2 BOTTLE, SPRAY in 1 CARTON (41167-5800-2) > 120 SPRAY, METERED in 1 BOTTLE, SPRAY

Profile for product number 002

Active Rx/OTC/Discontinued:OTCDosage:SPRAY, METERED;NASALStrength0.055MG/SPRAY
Approval Date:Oct 11, 2013TE:RLD:Yes

Expired US Patents for NDA 020468

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Sanofi Aventis Us NASACORT ALLERGY 24 HOUR triamcinolone acetonide SPRAY, METERED;NASAL 020468-002 Oct 11, 2013 ➤ Sign Up ➤ Sign Up
Sanofi Aventis Us NASACORT ALLERGY 24 HOUR triamcinolone acetonide SPRAY, METERED;NASAL 020468-002 Oct 11, 2013 ➤ Sign Up ➤ Sign Up
Sanofi Aventis Us NASACORT ALLERGY 24 HOUR triamcinolone acetonide SPRAY, METERED;NASAL 020468-002 Oct 11, 2013 ➤ Sign Up ➤ Sign Up
Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration

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