Loratadine - 56062-526-69 - (Loratadine)

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Drug Information of Loratadine

Product NDC: 56062-526
Proprietary Name: 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 Loratadine

Product NDC: 56062-526
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076134
Marketing Category: ANDA
Start Marketing Date: 20030819

Package Information of Loratadine

Package NDC: 56062-526-69
Package Description: 10 TABLET in 1 BLISTER PACK (56062-526-69)

NDC Information of Loratadine

NDC Code 56062-526-69
Proprietary Name Loratadine
Package Description 10 TABLET in 1 BLISTER PACK (56062-526-69)
Product NDC 56062-526
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 Publix Super Markets Inc
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Loratadine


General Information