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Levocetirizine Dihydrochloride - 31722-551-90 - (Levocetirizine Dihydrochloride)

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Drug Information of Levocetirizine Dihydrochloride

Product NDC: 31722-551
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
Coding System: National Drug Codes(NDC)

Labeler Information of Levocetirizine Dihydrochloride

Product NDC: 31722-551
Labeler Name: Camber Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091264
Marketing Category: ANDA
Start Marketing Date: 20120629

Package Information of Levocetirizine Dihydrochloride

Package NDC: 31722-551-90
Package Description: 90 TABLET in 1 BOTTLE (31722-551-90)

NDC Information of Levocetirizine Dihydrochloride

NDC Code 31722-551-90
Proprietary Name Levocetirizine Dihydrochloride
Package Description 90 TABLET in 1 BOTTLE (31722-551-90)
Product NDC 31722-551
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levocetirizine Dihydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120629
Marketing Category Name ANDA
Labeler Name Camber Pharmaceuticals, Inc.
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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