IBUPROFEN- ibuprofen tablet, film coated 
REMEDYREPACK INC.

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IBUPROFEN 400 MG - 600 MG AND 800 MG TABLETS

1. ibuprofen tablets 400 mg - 600 mg- 800 mg medguide

Repackaged By / Distributed By: RemedyRepack Inc.

625 Kolter Drive, Indiana, PA 15701

(724) 465-8762

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

NDC: 70518-0005-00

NDC: 70518-0005-01

NDC: 70518-0005-02

NDC: 70518-0005-03

NDC: 70518-0005-04

NDC: 70518-0005-05

NDC: 70518-0005-06

PACKAGING: 21 in 1 BLISTER PACK

PACKAGING: 14 in 1 BLISTER PACK

PACKAGING: 30 in 1 BLISTER PACK

PACKAGING: 10 in 1 BLISTER PACK

PACKAGING: 90 in 1 BOTTLE PLASTIC

PACKAGING: 30 in 1 BOTTLE PLASTIC

PACKAGING: 30 in 1 BLISTER PACK

Repackaged and Distributed By:

Remedy Repack, Inc.

625 Kolter Dr. Suite #4 Indiana, PA 1-724-465-8762

PRINCIPAL DISPLAY PANEL

DRUG: IBUPROFEN

GENERIC: IBUPROFEN

DOSAGE: TABLET, FILM COATED

ADMINSTRATION: ORAL

NDC: 70518-0005-0

NDC: 70518-0005-1

NDC: 70518-0005-2

NDC: 70518-0005-3

NDC: 70518-0005-4

NDC: 70518-0005-5

NDC: 70518-0005-6

COLOR: white

SHAPE: CAPSULE

SCORE: No score

SIZE: 19 mm

IMPRINT: 123

PACKAGING: 21 in 1 BLISTER PACK

PACKAGING: 14 in 1 BLISTER PACK

PACKAGING: 30 in 1 BLISTER PACK

PACKAGING: 10 in 1 BLISTER PACK

PACKAGING: 90 in 1 BOTTLE PLASTIC

PACKAGING: 30 in 1 BOTTLE PLASTIC

PACKAGING: 30 in 1 BLISTER PACK

ACTIVE INGREDIENT(S):

INACTIVE INGREDIENT(S):

MM7

IBUPROFEN 
ibuprofen tablet, film coated
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70518-0005(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:70518-0005-021 in 1 BLISTER PACK; Type 0: Not a Combination Product11/17/201606/04/2018
2NDC:70518-0005-114 in 1 BLISTER PACK; Type 0: Not a Combination Product12/05/201606/01/2018
3NDC:70518-0005-230 in 1 BLISTER PACK; Type 0: Not a Combination Product12/13/201606/11/2018
4NDC:70518-0005-310 in 1 BLISTER PACK; Type 0: Not a Combination Product01/27/201706/11/2018
5NDC:70518-0005-490 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/06/201703/30/2021
6NDC:70518-0005-530 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/04/201706/28/2018
7NDC:70518-0005-630 in 1 BLISTER PACK; Type 0: Not a Combination Product03/17/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA09079611/17/2016
Labeler - REMEDYREPACK INC. (829572556)

Revised: 1/2024
Document Id: 0e0ca589-8349-495b-e063-6394a90afbd0
Set id: 9dfc752f-3f66-4c39-bfa8-db6de9a9a9bf
Version: 14
Effective Time: 20240103
 
REMEDYREPACK INC.