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Losartan Potassium - 0615-7604-39 - (Losartan Potassium)

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Drug Information of Losartan Potassium

Product NDC: 0615-7604
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: 0615-7604
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076958
Marketing Category: ANDA
Start Marketing Date: 20101228

Package Information of Losartan Potassium

Package NDC: 0615-7604-39
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7604-39)

NDC Information of Losartan Potassium

NDC Code 0615-7604-39
Proprietary Name Losartan Potassium
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7604-39)
Product NDC 0615-7604
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Losartan Potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101228
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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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