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Loratadine and Pseudoephedrine - 54868-5656-2 - (loratadine and pseudoephedrine)

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Drug Information of Loratadine and Pseudoephedrine

Product NDC: 54868-5656
Proprietary Name: Loratadine and Pseudoephedrine
Non Proprietary Name: loratadine and pseudoephedrine
Active Ingredient(s): 10; 240    mg/1; mg/1 & nbsp;   loratadine and pseudoephedrine
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Loratadine and Pseudoephedrine

Product NDC: 54868-5656
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076557
Marketing Category: ANDA
Start Marketing Date: 20080527

Package Information of Loratadine and Pseudoephedrine

Package NDC: 54868-5656-2
Package Description: 3 BLISTER PACK in 1 CARTON (54868-5656-2) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Loratadine and Pseudoephedrine

NDC Code 54868-5656-2
Proprietary Name Loratadine and Pseudoephedrine
Package Description 3 BLISTER PACK in 1 CARTON (54868-5656-2) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 54868-5656
Product Type Name HUMAN OTC DRUG
Non Proprietary Name loratadine and pseudoephedrine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080527
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name LORATADINE; PSEUDOEPHEDRINE SULFATE
Strength Number 10; 240
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Loratadine and Pseudoephedrine


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