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berkley and jensen loratadine - 68391-612-87 - (Loratadine)

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Drug Information of berkley and jensen loratadine

Product NDC: 68391-612
Proprietary Name: berkley and jensen loratadine
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 berkley and jensen loratadine

Product NDC: 68391-612
Labeler Name: BJWC
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076301
Marketing Category: ANDA
Start Marketing Date: 20090417

Package Information of berkley and jensen loratadine

Package NDC: 68391-612-87
Package Description: 1 BOTTLE in 1 PACKAGE (68391-612-87) > 300 TABLET in 1 BOTTLE

NDC Information of berkley and jensen loratadine

NDC Code 68391-612-87
Proprietary Name berkley and jensen loratadine
Package Description 1 BOTTLE in 1 PACKAGE (68391-612-87) > 300 TABLET in 1 BOTTLE
Product NDC 68391-612
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090417
Marketing Category Name ANDA
Labeler Name BJWC
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of berkley and jensen loratadine


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