Loratadine - 53329-651-33 - (Loratadine)

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Drug Information of Loratadine

Product NDC: 53329-651
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: 53329-651
Labeler Name: Medline Industries, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076134
Marketing Category: ANDA
Start Marketing Date: 20030819

Package Information of Loratadine

Package NDC: 53329-651-33
Package Description: 30 TABLET in 1 BOTTLE (53329-651-33)

NDC Information of Loratadine

NDC Code 53329-651-33
Proprietary Name Loratadine
Package Description 30 TABLET in 1 BOTTLE (53329-651-33)
Product NDC 53329-651
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 Medline Industries, Inc.
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Loratadine


General Information