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allergy relief - 56062-571-39 - (fexofenadine hcl)

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Drug Information of allergy relief

Product NDC: 56062-571
Proprietary Name: allergy relief
Non Proprietary Name: fexofenadine hcl
Active Ingredient(s): 180    mg/1 & nbsp;   fexofenadine hcl
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of allergy relief

Product NDC: 56062-571
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076447
Marketing Category: ANDA
Start Marketing Date: 20120130

Package Information of allergy relief

Package NDC: 56062-571-39
Package Description: 1 BOTTLE in 1 CARTON (56062-571-39) > 30 TABLET, FILM COATED in 1 BOTTLE

NDC Information of allergy relief

NDC Code 56062-571-39
Proprietary Name allergy relief
Package Description 1 BOTTLE in 1 CARTON (56062-571-39) > 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC 56062-571
Product Type Name HUMAN OTC DRUG
Non Proprietary Name fexofenadine hcl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120130
Marketing Category Name ANDA
Labeler Name Publix Super Markets Inc
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of allergy relief


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