Prescription Drug Information: IBUPROFEN

IBUPROFEN- ibuprofen tablet, film coated
PD-Rx Pharmaceuticals, Inc.

ibuprofen tablets 400 mg — 600 mg- 800 mg medguide

MEDGUIDE IBUPROFEN TABLETS
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HOW SUPPLIED

600mg (white to off white, capsule shaped, biconvex, film coated tablets debossed with ‘122’ on one side and plain on the other side) Bottles of 30 NDC 43063-936-30

600 mg label

image
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IBUPROFEN
ibuprofen tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:43063-936(NDC:49483-603)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IBUPROFEN (IBUPROFEN) IBUPROFEN 600 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE
CROSCARMELLOSE SODIUM
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
POLYETHYLENE GLYCOL, UNSPECIFIED
POLYVINYL ALCOHOL
STARCH, PREGELATINIZED CORN
TALC
TITANIUM DIOXIDE
Product Characteristics
Color white Score no score
Shape CAPSULE Size 18mm
Flavor Imprint Code 122
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:43063-936-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090796 12/30/2015
Labeler — PD-Rx Pharmaceuticals, Inc. (156893695)
Registrant — PD-Rx Pharmaceuticals, Inc. (156893695)
Establishment
Name Address ID/FEI Operations
PD-Rx Pharmaceuticals, Inc. 156893695 repack (43063-936)

Revised: 08/2022 PD-Rx Pharmaceuticals, Inc.

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