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Loratadineantihistamine - 52125-600-08 - (Loratadine)

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Drug Information of Loratadineantihistamine

Product NDC: 52125-600
Proprietary Name: Loratadineantihistamine
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 Loratadineantihistamine

Product NDC: 52125-600
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076301
Marketing Category: ANDA
Start Marketing Date: 20130528

Package Information of Loratadineantihistamine

Package NDC: 52125-600-08
Package Description: 10 TABLET in 1 VIAL (52125-600-08)

NDC Information of Loratadineantihistamine

NDC Code 52125-600-08
Proprietary Name Loratadineantihistamine
Package Description 10 TABLET in 1 VIAL (52125-600-08)
Product NDC 52125-600
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Loratadine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130528
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Loratadineantihistamine


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