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Loratadine ODT - 59779-527-31 - (Loratadine)

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Drug Information of Loratadine ODT

Product NDC: 59779-527
Proprietary Name: Loratadine ODT
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 ODT

Product NDC: 59779-527
Labeler Name: CVS Pharmacy
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077153
Marketing Category: ANDA
Start Marketing Date: 20070927

Package Information of Loratadine ODT

Package NDC: 59779-527-31
Package Description: 1 BLISTER PACK in 1 CARTON (59779-527-31) > 30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of Loratadine ODT

NDC Code 59779-527-31
Proprietary Name Loratadine ODT
Package Description 1 BLISTER PACK in 1 CARTON (59779-527-31) > 30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 59779-527
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20070927
Marketing Category Name ANDA
Labeler Name CVS Pharmacy
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Loratadine ODT


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