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Equaline Allergy Relief - 41163-612-72 - (Loratadine)

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Drug Information of Equaline Allergy Relief

Product NDC: 41163-612
Proprietary Name: Equaline Allergy Relief
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 Equaline Allergy Relief

Product NDC: 41163-612
Labeler Name: Supervalu Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076301
Marketing Category: ANDA
Start Marketing Date: 20050207

Package Information of Equaline Allergy Relief

Package NDC: 41163-612-72
Package Description: 1 BOTTLE in 1 CARTON (41163-612-72) > 60 TABLET in 1 BOTTLE

NDC Information of Equaline Allergy Relief

NDC Code 41163-612-72
Proprietary Name Equaline Allergy Relief
Package Description 1 BOTTLE in 1 CARTON (41163-612-72) > 60 TABLET in 1 BOTTLE
Product NDC 41163-612
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050207
Marketing Category Name ANDA
Labeler Name Supervalu Inc
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Equaline Allergy Relief


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