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Losortan Potassium - 68084-347-01 - (Losartan Potassium)

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Drug Information of Losortan Potassium

Product NDC: 68084-347
Proprietary Name: Losortan 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 Losortan Potassium

Product NDC: 68084-347
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078243
Marketing Category: ANDA
Start Marketing Date: 20130613

Package Information of Losortan Potassium

Package NDC: 68084-347-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-347-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-347-11)

NDC Information of Losortan Potassium

NDC Code 68084-347-01
Proprietary Name Losortan Potassium
Package Description 10 BLISTER PACK in 1 CARTON (68084-347-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-347-11)
Product NDC 68084-347
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Losartan Potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130613
Marketing Category Name ANDA
Labeler Name American Health Packaging
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 Losortan Potassium


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