IBUPROFEN

IBUPROFEN- ibuprofen tablet, film coated
A-S Medication Solutions

ibuprofen tablets 400 mg — 600 mg- 800 mg medguide

MEDGUIDE IBUPROFEN TABLETS
(click image for full-size original)

HOW SUPPLIED

Product: 50090-5160

NDC: 50090-5160-0 16 TABLET, FILM COATED in a BOTTLE

IBUPROFEN TABLET, FILM COATED

Label ImageLabel Image
IBUPROFEN
ibuprofen tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50090-5160(NDC:49483-602)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IBUPROFEN (IBUPROFEN) IBUPROFEN 400 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE
CROSCARMELLOSE SODIUM
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
POLYETHYLENE GLYCOL, UNSPECIFIED
POLYVINYL ALCOHOL, UNSPECIFIED
STARCH, CORN
TALC
TITANIUM DIOXIDE
Product Characteristics
Color white Score no score
Shape ROUND Size 13mm
Flavor Imprint Code 121
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50090-5160-0 16 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090796 12/30/2015
Labeler — A-S Medication Solutions (830016429)
Establishment
Name Address ID/FEI Operations
A-S Medication Solutions 830016429 RELABEL (50090-5160), REPACK (50090-5160)

Revised: 01/2021 A-S Medication Solutions

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