Loratadine - 0781-5077-01 - (Loratadine)

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Drug Information of Loratadine

Product NDC: 0781-5077
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: 0781-5077
Labeler Name: Sandoz Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075209
Marketing Category: ANDA
Start Marketing Date: 20030121

Package Information of Loratadine

Package NDC: 0781-5077-01
Package Description: 100 TABLET in 1 BOTTLE (0781-5077-01)

NDC Information of Loratadine

NDC Code 0781-5077-01
Proprietary Name Loratadine
Package Description 100 TABLET in 1 BOTTLE (0781-5077-01)
Product NDC 0781-5077
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030121
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Loratadine


General Information