Home > National Drug Code (NDC) > Losartan Potassium

Losartan Potassium - 68788-9712-3 - (Losartan Potassium)

Alphabetical Index


Drug Information of Losartan Potassium

Product NDC: 68788-9712
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: 68788-9712
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090083
Marketing Category: ANDA
Start Marketing Date: 20130125

Package Information of Losartan Potassium

Package NDC: 68788-9712-3
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (68788-9712-3)

NDC Information of Losartan Potassium

NDC Code 68788-9712-3
Proprietary Name Losartan Potassium
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (68788-9712-3)
Product NDC 68788-9712
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Losartan Potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130125
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc.
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


General Information