Loratadine - 61715-017-51 - (Loratadine)

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Drug Information of Loratadine

Product NDC: 61715-017
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: 61715-017
Labeler Name: Kinray
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076134
Marketing Category: ANDA
Start Marketing Date: 20030819

Package Information of Loratadine

Package NDC: 61715-017-51
Package Description: 100 TABLET in 1 BOTTLE (61715-017-51)

NDC Information of Loratadine

NDC Code 61715-017-51
Proprietary Name Loratadine
Package Description 100 TABLET in 1 BOTTLE (61715-017-51)
Product NDC 61715-017
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 Kinray
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Loratadine


General Information