LOSARTAN POTASSIUM 25 Mg (Page 8 of 8)

LOSARTAN POTASSIUM

Label ImageLabel Image
LOSARTAN POTASSIUM 25 MG losartan potassium tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50090-5406(NDC:64380-933)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LOSARTAN POTASSIUM (LOSARTAN) LOSARTAN POTASSIUM 25 mg
Inactive Ingredients
Ingredient Name Strength
CROSCARMELLOSE SODIUM
HYPROMELLOSE, UNSPECIFIED
MAGNESIUM STEARATE
MANNITOL
MICROCRYSTALLINE CELLULOSE
POVIDONE, UNSPECIFIED
PROPYLENE GLYCOL
TALC
TITANIUM DIOXIDE
Product Characteristics
Color WHITE Score no score
Shape ROUND (Round, Biconvex) Size 8mm
Flavor Imprint Code 11
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50090-5406-0 30 TABLET, FILM COATED in 1 BOTTLE None
2 NDC:50090-5406-1 90 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090382 10/09/2019
Labeler — A-S Medication Solutions (830016429)
Establishment
Name Address ID/FEI Operations
A-S Medication Solutions 830016429 RELABEL (50090-5406), REPACK (50090-5406)

Revised: 03/2021 A-S Medication Solutions

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