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LOSARTAN POTASSIUM - 16571-500-11 - (LOSARTAN POTASSIUM)

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Drug Information of LOSARTAN POTASSIUM

Product NDC: 16571-500
Proprietary Name: LOSARTAN POTASSIUM
Non Proprietary Name: LOSARTAN POTASSIUM
Active Ingredient(s): 25    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: 16571-500
Labeler Name: PACK Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091497
Marketing Category: ANDA
Start Marketing Date: 20110601

Package Information of LOSARTAN POTASSIUM

Package NDC: 16571-500-11
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (16571-500-11)

NDC Information of LOSARTAN POTASSIUM

NDC Code 16571-500-11
Proprietary Name LOSARTAN POTASSIUM
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (16571-500-11)
Product NDC 16571-500
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LOSARTAN POTASSIUM
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110601
Marketing Category Name ANDA
Labeler Name PACK Pharmaceuticals, LLC
Substance Name LOSARTAN POTASSIUM
Strength Number 25
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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