Losartan Potassium (Page 8 of 8)

Losartan Potassium 25mg Tablets

Label Image
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LOSARTAN POTASSIUM losartan potassium tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53002-5624(NDC:65862-201)
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
MICROCRYSTALLINE CELLULOSE
LACTOSE MONOHYDRATE
STARCH, CORN
LOW-SUBSTITUTED HYDROXYPROPYL CELLULOSE, UNSPECIFIED
MAGNESIUM STEARATE
HYDROXYPROPYL CELLULOSE (1600000 WAMW)
HYPROMELLOSE 2910 (6 MPA.S)
TITANIUM DIOXIDE
FD&C BLUE NO. 2
D&C YELLOW NO. 10
WATER
Product Characteristics
Color GREEN Score no score
Shape OVAL (Biconvex) Size 8mm
Flavor Imprint Code E;45
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53002-5624-9 90 TABLET, FILM COATED in 1 BOTTLE None
2 NDC:53002-5624-0 100 TABLET, FILM COATED in 1 BOTTLE None
3 NDC:53002-5624-3 30 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090083 10/06/2010
Labeler — RPK Pharmaceuticals, Inc. (147096275)
Establishment
Name Address ID/FEI Operations
RPK Pharmaceuticals, Inc. 147096275 RELABEL (53002-5624), REPACK (53002-5624)

Revised: 01/2021 RPK Pharmaceuticals, Inc.

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