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up and up allergy relief - 11673-612-76 - (Loratadine)

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Drug Information of up and up allergy relief

Product NDC: 11673-612
Proprietary Name: up and up 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 up and up allergy relief

Product NDC: 11673-612
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076301
Marketing Category: ANDA
Start Marketing Date: 20120326

Package Information of up and up allergy relief

Package NDC: 11673-612-76
Package Description: 1 BOTTLE in 1 CARTON (11673-612-76) > 120 TABLET in 1 BOTTLE

NDC Information of up and up allergy relief

NDC Code 11673-612-76
Proprietary Name up and up allergy relief
Package Description 1 BOTTLE in 1 CARTON (11673-612-76) > 120 TABLET in 1 BOTTLE
Product NDC 11673-612
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120326
Marketing Category Name ANDA
Labeler Name Target Corporation
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of up and up allergy relief


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