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Losartan potassium - 33342-045-12 - (Losartan potassium)

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Drug Information of Losartan potassium

Product NDC: 33342-045
Proprietary Name: Losartan potassium
Non Proprietary Name: Losartan potassium
Active Ingredient(s): 50    mg/1 & nbsp;   Losartan potassium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Losartan potassium

Product NDC: 33342-045
Labeler Name: Macleods Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202230
Marketing Category: ANDA
Start Marketing Date: 20120601

Package Information of Losartan potassium

Package NDC: 33342-045-12
Package Description: 10 BLISTER PACK in 1 CARTON (33342-045-12) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Losartan potassium

NDC Code 33342-045-12
Proprietary Name Losartan potassium
Package Description 10 BLISTER PACK in 1 CARTON (33342-045-12) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 33342-045
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Losartan potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120601
Marketing Category Name ANDA
Labeler Name Macleods Pharmaceuticals Limited
Substance Name LOSARTAN POTASSIUM
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of Losartan potassium


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