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up and up allergy relief - 11673-571-39 - (fexofenadine hydrochloride)

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Drug Information of up and up allergy relief

Product NDC: 11673-571
Proprietary Name: up and up allergy relief
Non Proprietary Name: fexofenadine hydrochloride
Active Ingredient(s): 180    mg/1 & nbsp;   fexofenadine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of up and up allergy relief

Product NDC: 11673-571
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076447
Marketing Category: ANDA
Start Marketing Date: 20110413

Package Information of up and up allergy relief

Package NDC: 11673-571-39
Package Description: 1 BOTTLE in 1 CARTON (11673-571-39) > 30 TABLET, FILM COATED in 1 BOTTLE

NDC Information of up and up allergy relief

NDC Code 11673-571-39
Proprietary Name up and up allergy relief
Package Description 1 BOTTLE in 1 CARTON (11673-571-39) > 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC 11673-571
Product Type Name HUMAN OTC DRUG
Non Proprietary Name fexofenadine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110413
Marketing Category Name ANDA
Labeler Name Target Corporation
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of up and up allergy relief


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