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Loratadine and Pseudoephedrine - 21695-729-05 - (loratadine and pseudoephedrine)

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Drug Information of Loratadine and Pseudoephedrine

Product NDC: 21695-729
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: 21695-729
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076557
Marketing Category: ANDA
Start Marketing Date: 20041117

Package Information of Loratadine and Pseudoephedrine

Package NDC: 21695-729-05
Package Description: 5 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-729-05)

NDC Information of Loratadine and Pseudoephedrine

NDC Code 21695-729-05
Proprietary Name Loratadine and Pseudoephedrine
Package Description 5 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-729-05)
Product NDC 21695-729
Product Type Name HUMAN OTC DRUG
Non Proprietary Name loratadine and pseudoephedrine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20041117
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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