Loratadine - 36800-527-69 - (Loratadine)

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Drug Information of Loratadine

Product NDC: 36800-527
Proprietary Name: Loratadine
Non Proprietary Name: Loratadine
Active Ingredient(s): 10    mg/1 & nbsp;   Loratadine
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Loratadine

Product NDC: 36800-527
Labeler Name: Topcare Associates LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077153
Marketing Category: ANDA
Start Marketing Date: 20070831

Package Information of Loratadine

Package NDC: 36800-527-69
Package Description: 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (36800-527-69)

NDC Information of Loratadine

NDC Code 36800-527-69
Proprietary Name Loratadine
Package Description 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (36800-527-69)
Product NDC 36800-527
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20070831
Marketing Category Name ANDA
Labeler Name Topcare Associates LLC
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Loratadine


General Information