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Losartan Potassium - 0781-5805-10 - (losartan potassium)

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Drug Information of Losartan Potassium

Product NDC: 0781-5805
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: 0781-5805
Labeler Name: Sandoz Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020386
Marketing Category: NDA
Start Marketing Date: 19950414

Package Information of Losartan Potassium

Package NDC: 0781-5805-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (0781-5805-10)

NDC Information of Losartan Potassium

NDC Code 0781-5805-10
Proprietary Name Losartan Potassium
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (0781-5805-10)
Product NDC 0781-5805
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name losartan potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19950414
Marketing Category Name NDA
Labeler Name Sandoz Inc.
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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