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

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 20 NDC 68788-7745-02
Bottles of 28 NDC 68788-7745-08
Bottles of 30 NDC 68788-7745-03
Bottles of 50 NDC 68788-7745-05
Bottles of 60 NDC 68788-7745-06
Bottles of 90 NDC 68788-7745-09
Bottles of 100 NDC 68788-7745-01

Repackaged by Preferred Pharmaceuticals, Inc.

400mg Ibuprofen

Ibuprofen Tablets USP 400mg
IBUPROFEN 
ibuprofen tablet, film coated
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:68788-7745(NDC:49483-602)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN400 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
ShapeROUNDSize13mm
FlavorImprint Code 121
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68788-7745-220 in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
2NDC:68788-7745-828 in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
3NDC:68788-7745-330 in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
4NDC:68788-7745-550 in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
5NDC:68788-7745-660 in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
6NDC:68788-7745-990 in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
7NDC:68788-7745-1100 in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA09079607/01/2020
Labeler - Preferred Pharmaceuticals, Inc. (791119022)
Registrant - Preferred Pharmaceuticals, Inc. (791119022)
Establishment
NameAddressID/FEIBusiness Operations
Preferred Pharmaceuticals, Inc.791119022REPACK(68788-7745)

Revised: 7/2023
Document Id: eae45ecc-731a-418e-8a94-cef595fb83c3
Set id: 20fda75a-c560-428b-b9fd-c12e97df4a74
Version: 4
Effective Time: 20230713
 
Preferred Pharmaceuticals, Inc.