Loratadine - 55154-5424-9 - (Loratadine)

Alphabetical Index


Drug Information of Loratadine

Product NDC: 55154-5424
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: 55154-5424
Labeler Name: Cardinal Health
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075209
Marketing Category: ANDA
Start Marketing Date: 20030121

Package Information of Loratadine

Package NDC: 55154-5424-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-5424-9) > 5 TABLET in 1 BLISTER PACK

NDC Information of Loratadine

NDC Code 55154-5424-9
Proprietary Name Loratadine
Package Description 6 BLISTER PACK in 1 CARTON (55154-5424-9) > 5 TABLET in 1 BLISTER PACK
Product NDC 55154-5424
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 Cardinal Health
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Loratadine


General Information