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Loratadine D - 45802-106-60 - (Loratadine, Pseudoephedrine)

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Drug Information of Loratadine D

Product NDC: 45802-106
Proprietary Name: Loratadine D
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 Loratadine D

Product NDC: 45802-106
Labeler Name: Perrigo New York Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076050
Marketing Category: ANDA
Start Marketing Date: 20120119

Package Information of Loratadine D

Package NDC: 45802-106-60
Package Description: 2 BLISTER PACK in 1 CARTON (45802-106-60) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Loratadine D

NDC Code 45802-106-60
Proprietary Name Loratadine D
Package Description 2 BLISTER PACK in 1 CARTON (45802-106-60) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 45802-106
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine, Pseudoephedrine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120119
Marketing Category Name ANDA
Labeler Name Perrigo New York Inc
Substance Name LORATADINE; PSEUDOEPHEDRINE SULFATE
Strength Number 5; 120
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Loratadine D


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