IBUPROFEN

IBUPROFEN- ibuprofen tablet, film coated
Preferred Pharmaceuticals Inc.

ibuprofen tablets 400 mg — 600 mg- 800 mg medguide

MEDGUIDE IBUPROFEN TABLETS
(click image for full-size original)

HOW SUPPLIED

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

Bottles of 14 NDC 68788-7079-4
Bottles of 20 NDC 68788-7079-2
Bottles of 21 NDC 68788-7079-7
Bottles of 30 NDC 68788-7079-3
Bottles of 50 NDC 68788-7079-5
Bottles of 60 NDC 68788-7079-6
Bottles of 90 NDC 68788-7079-9
Bottles of 100 NDC 68788-7079-1
Bottles of 120 NDC 68788-7079-8

Repackaged By: Preferred Pharmaceuticals Inc.

800mg LABEL

Ibuprofen Tablets USP 800mg
(click image for full-size original)
IBUPROFEN
ibuprofen tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68788-7079(NDC:49483-604)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IBUPROFEN (IBUPROFEN) IBUPROFEN 800 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE
CROSCARMELLOSE SODIUM
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
POLYETHYLENE GLYCOL, UNSPECIFIED
POLYVINYL ALCOHOL, UNSPECIFIED
STARCH, CORN
TALC
TITANIUM DIOXIDE
Product Characteristics
Color white Score no score
Shape CAPSULE Size 19mm
Flavor Imprint Code 123
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68788-7079-4 14 TABLET, FILM COATED in 1 BOTTLE None
2 NDC:68788-7079-2 20 TABLET, FILM COATED in 1 BOTTLE None
3 NDC:68788-7079-7 21 TABLET, FILM COATED in 1 BOTTLE None
4 NDC:68788-7079-3 30 TABLET, FILM COATED in 1 BOTTLE None
5 NDC:68788-7079-5 50 TABLET, FILM COATED in 1 BOTTLE None
6 NDC:68788-7079-6 60 TABLET, FILM COATED in 1 BOTTLE None
7 NDC:68788-7079-9 90 TABLET, FILM COATED in 1 BOTTLE None
8 NDC:68788-7079-1 100 TABLET, FILM COATED in 1 BOTTLE None
9 NDC:68788-7079-8 120 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090796 06/17/2020
Labeler — Preferred Pharmaceuticals Inc. (791119022)
Registrant — Preferred Pharmaceuticals Inc. (791119022)
Establishment
Name Address ID/FEI Operations
Preferred Pharmaceuticals Inc. 791119022 REPACK (68788-7079)

Revised: 06/2021 Preferred Pharmaceuticals Inc.

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