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Allergy Relief d 12 - 59779-013-60 - (Loratadine, Pseudoephedrine)

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Drug Information of Allergy Relief d 12

Product NDC: 59779-013
Proprietary Name: Allergy Relief d 12
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 Allergy Relief d 12

Product NDC: 59779-013
Labeler Name: CVS Pharmacy
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076050
Marketing Category: ANDA
Start Marketing Date: 20120125

Package Information of Allergy Relief d 12

Package NDC: 59779-013-60
Package Description: 2 BLISTER PACK in 1 CARTON (59779-013-60) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Allergy Relief d 12

NDC Code 59779-013-60
Proprietary Name Allergy Relief d 12
Package Description 2 BLISTER PACK in 1 CARTON (59779-013-60) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 59779-013
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine, Pseudoephedrine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120125
Marketing Category Name ANDA
Labeler Name CVS Pharmacy
Substance Name LORATADINE; PSEUDOEPHEDRINE SULFATE
Strength Number 5; 120
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Allergy Relief d 12


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