Loratadine - 54838-554-40 - (Loratadine)

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Drug Information of Loratadine

Product NDC: 54838-554
Proprietary Name: Loratadine
Non Proprietary Name: Loratadine
Active Ingredient(s): 5    mg/5mL & nbsp;   Loratadine
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Loratadine

Product NDC: 54838-554
Labeler Name: Silarx Pharmaceuticals, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077421
Marketing Category: ANDA
Start Marketing Date: 20101124

Package Information of Loratadine

Package NDC: 54838-554-40
Package Description: 120 mL in 1 CARTON (54838-554-40)

NDC Information of Loratadine

NDC Code 54838-554-40
Proprietary Name Loratadine
Package Description 120 mL in 1 CARTON (54838-554-40)
Product NDC 54838-554
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20101124
Marketing Category Name ANDA
Labeler Name Silarx Pharmaceuticals, Inc
Substance Name LORATADINE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Loratadine


General Information