LOSARTAN POTASSIUM 50 Mg (Page 8 of 8)

Principal Display Panel

NDC: 51655-418-26

Label
(click image for full-size original)
LOSARTAN POTASSIUM 50 MG losartan potassium tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:51655-418(NDC:64380-934)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LOSARTAN POTASSIUM (LOSARTAN) LOSARTAN POTASSIUM 50 mg
Inactive Ingredients
Ingredient Name Strength
CROSCARMELLOSE SODIUM
HYPROMELLOSES
MAGNESIUM STEARATE
MANNITOL
CELLULOSE, MICROCRYSTALLINE
POVIDONE
PROPYLENE GLYCOL
TALC
TITANIUM DIOXIDE
Product Characteristics
Color white Score 2 pieces
Shape ROUND (Round, Biconvex) Size 10mm
Flavor Imprint Code 12
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:51655-418-26 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090382 07/15/2020
Labeler — Northwind Pharmaceuticals (036986393)
Registrant — Northwind Pharmaceuticals (036986393)
Establishment
Name Address ID/FEI Operations
Northwind Pharmaceuticals 036986393 repack (51655-418)

Revised: 05/2021 Northwind Pharmaceuticals

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