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Sunmark Loratadine ODT - 49348-930-01 - (Loratadine)

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Drug Information of Sunmark Loratadine ODT

Product NDC: 49348-930
Proprietary Name: Sunmark 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 Sunmark Loratadine ODT

Product NDC: 49348-930
Labeler Name: Sunmark
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077153
Marketing Category: ANDA
Start Marketing Date: 20070831

Package Information of Sunmark Loratadine ODT

Package NDC: 49348-930-01
Package Description: 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49348-930-01)

NDC Information of Sunmark Loratadine ODT

NDC Code 49348-930-01
Proprietary Name Sunmark Loratadine ODT
Package Description 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49348-930-01)
Product NDC 49348-930
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 Sunmark
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Sunmark Loratadine ODT


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