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LEADER Loratadine - 37205-346-72 - (loratadine)

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Drug Information of LEADER Loratadine

Product NDC: 37205-346
Proprietary Name: LEADER Loratadine
Non Proprietary Name: loratadine
Active Ingredient(s): 10    mg/1 & nbsp;   loratadine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of LEADER Loratadine

Product NDC: 37205-346
Labeler Name: Cardinal Health
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076134
Marketing Category: ANDA
Start Marketing Date: 20030819

Package Information of LEADER Loratadine

Package NDC: 37205-346-72
Package Description: 60 TABLET in 1 BOTTLE (37205-346-72)

NDC Information of LEADER Loratadine

NDC Code 37205-346-72
Proprietary Name LEADER Loratadine
Package Description 60 TABLET in 1 BOTTLE (37205-346-72)
Product NDC 37205-346
Product Type Name HUMAN OTC DRUG
Non Proprietary Name loratadine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030819
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of LEADER Loratadine


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