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Up and Up allergy and congestion relief - 11673-013-39 - (Loratadine, Pseudoephedrine)

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Drug Information of Up and Up allergy and congestion relief

Product NDC: 11673-013
Proprietary Name: Up and Up allergy and congestion relief
Non Proprietary Name: Loratadine, Pseudoephedrine
Active Ingredient(s): 5; 120    mg/1; mg/1 & nbsp;   Loratadine, Pseudoephedrine
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Up and Up allergy and congestion relief

Product NDC: 11673-013
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076050
Marketing Category: ANDA
Start Marketing Date: 20120312

Package Information of Up and Up allergy and congestion relief

Package NDC: 11673-013-39
Package Description: 3 BLISTER PACK in 1 CARTON (11673-013-39) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Up and Up allergy and congestion relief

NDC Code 11673-013-39
Proprietary Name Up and Up allergy and congestion relief
Package Description 3 BLISTER PACK in 1 CARTON (11673-013-39) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 11673-013
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine, Pseudoephedrine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120312
Marketing Category Name ANDA
Labeler Name Target Corporation
Substance Name LORATADINE; PSEUDOEPHEDRINE SULFATE
Strength Number 5; 120
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Up and Up allergy and congestion relief


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