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Loratadine ODT - 41250-527-31 - (Loratadine)

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Drug Information of Loratadine ODT

Product NDC: 41250-527
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: 41250-527
Labeler Name: Meijer Distribution, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077153
Marketing Category: ANDA
Start Marketing Date: 20070831

Package Information of Loratadine ODT

Package NDC: 41250-527-31
Package Description: 30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (41250-527-31)

NDC Information of Loratadine ODT

NDC Code 41250-527-31
Proprietary Name Loratadine ODT
Package Description 30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (41250-527-31)
Product NDC 41250-527
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 Meijer Distribution, Inc.
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Loratadine ODT


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