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Loratadine and Pseudoephedrine Sulfate - 49348-543-01 - (Loratadine and Pseudoephedrine Sulfate)

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Drug Information of Loratadine and Pseudoephedrine Sulfate

Product NDC: 49348-543
Proprietary Name: Loratadine and Pseudoephedrine Sulfate
Non Proprietary Name: Loratadine and Pseudoephedrine Sulfate
Active Ingredient(s): 10; 240    mg/1; mg/1 & nbsp;   Loratadine and Pseudoephedrine Sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Loratadine and Pseudoephedrine Sulfate

Product NDC: 49348-543
Labeler Name: Sunmark
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076557
Marketing Category: ANDA
Start Marketing Date: 20041117

Package Information of Loratadine and Pseudoephedrine Sulfate

Package NDC: 49348-543-01
Package Description: 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (49348-543-01)

NDC Information of Loratadine and Pseudoephedrine Sulfate

NDC Code 49348-543-01
Proprietary Name Loratadine and Pseudoephedrine Sulfate
Package Description 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (49348-543-01)
Product NDC 49348-543
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine and Pseudoephedrine Sulfate
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20041117
Marketing Category Name ANDA
Labeler Name Sunmark
Substance Name LORATADINE; PSEUDOEPHEDRINE SULFATE
Strength Number 10; 240
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Loratadine and Pseudoephedrine Sulfate


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