Furosemide (Page 4 of 4)

PRINCIPAL DISPLAY PANEL

NDC 50090-0150-0

Packaged by:
A-S Medication Solutions
Libertyville, IL 60048

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PRINCIPAL DISPLAY PANEL

NDC 50090-0152-0

Packaged by:
A-S Medication Solutions
Libertyville, IL 60048

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PRINCIPAL DISPLAY PANEL

NDC 50090-0154-0

Packaged by:
A-S Medication Solutions
Libertyville, IL 60048

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FUROSEMIDE
furosemide tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50090-0152(NDC:0781-1818)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FUROSEMIDE (FUROSEMIDE) FUROSEMIDE 20 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
STARCH, CORN
Product Characteristics
Color WHITE Score 2 pieces
Shape ROUND Size 6mm
Flavor Imprint Code GG21
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50090-0152-0 30 TABLET in 1 BOTTLE None
2 NDC:50090-0152-1 100 TABLET in 1 BOTTLE None
3 NDC:50090-0152-7 200 TABLET in 1 BOTTLE None
4 NDC:50090-0152-8 90 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018569 10/19/1981
FUROSEMIDE
furosemide tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50090-0154(NDC:0781-1966)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FUROSEMIDE (FUROSEMIDE) FUROSEMIDE 40 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
STARCH, CORN
Product Characteristics
Color WHITE Score 2 pieces
Shape ROUND Size 8mm
Flavor Imprint Code GG201
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50090-0154-0 30 TABLET in 1 BOTTLE None
2 NDC:50090-0154-1 100 TABLET in 1 BOTTLE None
3 NDC:50090-0154-2 15 TABLET in 1 BOTTLE None
4 NDC:50090-0154-3 60 TABLET in 1 BOTTLE None
5 NDC:50090-0154-9 90 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018569 10/19/1981
FUROSEMIDE
furosemide tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50090-0150(NDC:0781-1446)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FUROSEMIDE (FUROSEMIDE) FUROSEMIDE 80 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
STARCH, CORN
Product Characteristics
Color WHITE Score 2 pieces
Shape ROUND Size 10mm
Flavor Imprint Code GG80
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50090-0150-0 100 TABLET in 1 BOTTLE None
2 NDC:50090-0150-1 30 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018569 10/19/1981
Labeler — A-S Medication Solutions LLC (830016429)
Establishment
Name Address ID/FEI Operations
A-S Medication Solutions LLC 830016429 repack (50090-0150), repack (50090-0152), repack (50090-0154)

Revised: 02/2015 A-S Medication Solutions LLC

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