Loratadine - 63629-1329-3 - (Loratadine)

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Drug Information of Loratadine

Product NDC: 63629-1329
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: 63629-1329
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076301
Marketing Category: ANDA
Start Marketing Date: 20081015

Package Information of Loratadine

Package NDC: 63629-1329-3
Package Description: 60 TABLET in 1 BOTTLE (63629-1329-3)

NDC Information of Loratadine

NDC Code 63629-1329-3
Proprietary Name Loratadine
Package Description 60 TABLET in 1 BOTTLE (63629-1329-3)
Product NDC 63629-1329
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Loratadine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081015
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Loratadine


General Information