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levocetirizine dihydrochloride - 55111-282-30 - (levocetirizine dihydrochloride)

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Drug Information of levocetirizine dihydrochloride

Product NDC: 55111-282
Proprietary Name: levocetirizine dihydrochloride
Non Proprietary Name: levocetirizine dihydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   levocetirizine dihydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of levocetirizine dihydrochloride

Product NDC: 55111-282
Labeler Name: Dr.Reddy's laboratories Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090392
Marketing Category: ANDA
Start Marketing Date: 20110224

Package Information of levocetirizine dihydrochloride

Package NDC: 55111-282-30
Package Description: 30 TABLET, COATED in 1 BOTTLE (55111-282-30)

NDC Information of levocetirizine dihydrochloride

NDC Code 55111-282-30
Proprietary Name levocetirizine dihydrochloride
Package Description 30 TABLET, COATED in 1 BOTTLE (55111-282-30)
Product NDC 55111-282
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levocetirizine dihydrochloride
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20110224
Marketing Category Name ANDA
Labeler Name Dr.Reddy's laboratories Ltd.
Substance Name LEVOCETIRIZINE DIHYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

Complete Information of levocetirizine dihydrochloride


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