Loratadine - 52959-740-20 - (Loratadine)

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Drug Information of Loratadine

Product NDC: 52959-740
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: 52959-740
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076301
Marketing Category: ANDA
Start Marketing Date: 20081015

Package Information of Loratadine

Package NDC: 52959-740-20
Package Description: 20 TABLET in 1 BOTTLE (52959-740-20)

NDC Information of Loratadine

NDC Code 52959-740-20
Proprietary Name Loratadine
Package Description 20 TABLET in 1 BOTTLE (52959-740-20)
Product NDC 52959-740
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081015
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Loratadine


General Information