IBUPROFEN- ibuprofen tablet, film coated 
RedPharm Drug, Inc.

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IBUPROFEN 800mg

ibuprofen tablets 400 mg - 600 mg- 800 mg medguide

MEDGUIDE IBUPROFEN TABLETS

HOW SUPPLIED

400mg (white to of white, round, biconvex, film coated tablets debossed with '121' on one side and plain on the other side) Bottles of 100 & 500

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, 50, 100 & 500

800 mg (white to off-white, capsule shaped, biconvex, film-coated​ tablets debossed with ‘123’ on one side and plain on other side)

400mg Ibuprofen 100 count label

400 mg label

400 mg 500 count label

400 mg 500 count label

600 mg 100 count label

600 mg 100 count label

800 mg 100 count label

800 mg 100 count label

600 MG 500 COUNT LABEL

600 MG 500 CT LABEL

800 MG 500 COUNT LABEL

800 MG 500 COUNT LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

10 COUNT

IBUPROFEN 
ibuprofen tablet, film coated
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:67296-1756(NDC:49483-604)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN800 mg
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POLYVINYL ALCOHOL (UNII: 532B59J990)  
STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorwhiteScoreno score
ShapeCAPSULESize19mm
FlavorImprint Code 123
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67296-1756-330 in 1 BOTTLE; Type 0: Not a Combination Product01/01/2020
2NDC:67296-1756-110 in 1 BOTTLE; Type 0: Not a Combination Product01/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA09079601/01/2020
Labeler - RedPharm Drug, Inc. (828374897)
Establishment
NameAddressID/FEIBusiness Operations
RedPharm Drug, Inc.828374897repack(67296-1756)

Revised: 7/2024
Document Id: 1e1cbc06-5510-cbb2-e063-6294a90a5f4b
Set id: a2f3b793-171c-2bde-e053-2995a90a62a0
Version: 5
Effective Time: 20240725
 
RedPharm Drug, Inc.