IBUPROFEN- ibuprofen tablet, film coated 
Preferred Pharmaceuticals Inc.

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IBUPROFEN 400 MG - 600 MG AND 800 MG TABLETS

ibuprofen tablets 400 mg - 600 mg- 800 mg medguide

MEDGUIDE IBUPROFEN TABLETS
Repackaged By: Preferred Pharmaceuticals Inc.

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 14 NDC 68788-7602-4

Repackaged By: Preferred Pharmaceuticals Inc.

600mg Label

Ibuprofen Tablets 600mg
IBUPROFEN 
ibuprofen tablet, film coated
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:68788-7602(NDC:49483-603)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN600 mg
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
STARCH, CORN (UNII: O8232NY3SJ)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorwhiteScoreno score
ShapeCAPSULESize18mm
FlavorImprint Code 122
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68788-7602-414 in 1 BOTTLE; Type 0: Not a Combination Product02/14/202007/13/2023
2NDC:68788-7602-220 in 1 BOTTLE; Type 0: Not a Combination Product02/14/202007/13/2023
3NDC:68788-7602-721 in 1 BOTTLE; Type 0: Not a Combination Product02/14/202007/13/2023
4NDC:68788-7602-330 in 1 BOTTLE; Type 0: Not a Combination Product02/14/202007/13/2023
5NDC:68788-7602-550 in 1 BOTTLE; Type 0: Not a Combination Product02/14/202007/13/2023
6NDC:68788-7602-660 in 1 BOTTLE; Type 0: Not a Combination Product02/14/202007/13/2023
7NDC:68788-7602-990 in 1 BOTTLE; Type 0: Not a Combination Product02/14/202007/13/2023
8NDC:68788-7602-1100 in 1 BOTTLE; Type 0: Not a Combination Product02/14/202007/13/2023
9NDC:68788-7602-8120 in 1 BOTTLE; Type 0: Not a Combination Product02/14/202007/13/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA09079602/14/202007/13/2023
Labeler - Preferred Pharmaceuticals Inc. (791119022)
Registrant - Preferred Pharmaceuticals Inc. (791119022)
Establishment
NameAddressID/FEIBusiness Operations
Preferred Pharmaceuticals Inc.791119022REPACK(68788-7602)

Revised: 7/2023
Document Id: d83ca34e-c14d-41b0-a101-2d9fa4526b01
Set id: bd7d9986-f0ec-4013-8b57-6ce7cc013cf6
Version: 4
Effective Time: 20230713
 
Preferred Pharmaceuticals Inc.