Losartan Potassium and Hydrochlorothiazide (Page 10 of 10)

Package/Label Display Panel

63187-347-30
(click image for full-size original)
63187-347-30
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
losartan potassium and hydrochlorothiazide tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63187-347(NDC:0093-7368)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LOSARTAN POTASSIUM (LOSARTAN) LOSARTAN POTASSIUM 100 mg
HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) HYDROCHLOROTHIAZIDE 25 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
POLYETHYLENE GLYCOL 3350
POLYETHYLENE GLYCOL 4000
POLYVINYL ALCOHOL, UNSPECIFIED
STARCH, CORN
TALC
TITANIUM DIOXIDE
D&C YELLOW NO. 10
ALUMINUM OXIDE
Product Characteristics
Color YELLOW (light yellow) Score no score
Shape OVAL Size 15mm
Flavor Imprint Code 93;7368
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63187-347-30 30 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077157 04/06/2010
Labeler — Proficient Rx LP (079196022)
Establishment
Name Address ID/FEI Operations
Proficient Rx LP 079196022 REPACK (63187-347), RELABEL (63187-347)

Revised: 04/2021 Proficient Rx LP

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