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Losartan Potassium - 60505-3162-0 - (Losartan Potassium)

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Drug Information of Losartan Potassium

Product NDC: 60505-3162
Proprietary Name: Losartan Potassium
Non Proprietary Name: Losartan Potassium
Active Ingredient(s): 100    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: 60505-3162
Labeler Name: Apotex Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090790
Marketing Category: ANDA
Start Marketing Date: 20101003

Package Information of Losartan Potassium

Package NDC: 60505-3162-0
Package Description: 10 BLISTER PACK in 1 CARTON (60505-3162-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Losartan Potassium

NDC Code 60505-3162-0
Proprietary Name Losartan Potassium
Package Description 10 BLISTER PACK in 1 CARTON (60505-3162-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 60505-3162
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Losartan Potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101003
Marketing Category Name ANDA
Labeler Name Apotex Corp
Substance Name LOSARTAN POTASSIUM
Strength Number 100
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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