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Losartan Potassium - 76237-284-30 - (Losartan Potassium)

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Drug Information of Losartan Potassium

Product NDC: 76237-284
Proprietary Name: Losartan 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 Losartan Potassium

Product NDC: 76237-284
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076958
Marketing Category: ANDA
Start Marketing Date: 20130410

Package Information of Losartan Potassium

Package NDC: 76237-284-30
Package Description: 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-284-30) > 5 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Losartan Potassium

NDC Code 76237-284-30
Proprietary Name Losartan Potassium
Package Description 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-284-30) > 5 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 76237-284
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Losartan Potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130410
Marketing Category Name ANDA
Labeler Name McKesson Contract 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 Losartan Potassium


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