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allergy relief - 59779-612-72 - (Loratadine)

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Drug Information of allergy relief

Product NDC: 59779-612
Proprietary Name: allergy relief
Non Proprietary Name: Loratadine
Active Ingredient(s): 10    mg/1 & nbsp;   Loratadine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of allergy relief

Product NDC: 59779-612
Labeler Name: CVS Pharmacy
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076301
Marketing Category: ANDA
Start Marketing Date: 20050104

Package Information of allergy relief

Package NDC: 59779-612-72
Package Description: 1 BOTTLE in 1 CARTON (59779-612-72) > 60 TABLET in 1 BOTTLE

NDC Information of allergy relief

NDC Code 59779-612-72
Proprietary Name allergy relief
Package Description 1 BOTTLE in 1 CARTON (59779-612-72) > 60 TABLET in 1 BOTTLE
Product NDC 59779-612
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050104
Marketing Category Name ANDA
Labeler Name CVS Pharmacy
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of allergy relief


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