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Ibuprofen - Medication Information

Product NDC Code 72189-266
Drug Name

Ibuprofen

Type Generic
Pharm Class Anti-Inflammatory Agents,
Non-Steroidal [CS],
Cyclooxygenase Inhibitors [MoA],
Nonsteroidal Anti-inflammatory Drug [EPC]
Active Ingredients
Ibuprofen 800 mg/1
Route ORAL
Dosage Form TABLET, FILM COATED
RxCUI drug identifier 197806,
197807
Application Number ANDA090796
Labeler Name DIRECT RX
Packages
Package NDC Code Description
72189-266-15 15 tablet, film coated in 1 bottle (72189-266-15)
72189-266-30 30 tablet, film coated in 1 bottle (72189-266-30)
72189-266-40 40 tablet, film coated in 1 bottle (72189-266-40)
72189-266-60 60 tablet, film coated in 1 bottle (72189-266-60)
72189-266-71 100 tablet, film coated in 1 bottle (72189-266-71)
72189-266-72 120 tablet, film coated in 1 bottle (72189-266-72)
72189-266-90 90 tablet, film coated in 1 bottle (72189-266-90)
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Spl product data elements

Usually a list of ingredients in a drug product.
IBUPROFEN IBUPROFEN CROSCARMELLOSE SODIUM POLYVINYL ALCOHOL, UNSPECIFIED TITANIUM DIOXIDE SILICON DIOXIDE TALC STARCH, CORN POLYETHYLENE GLYCOL, UNSPECIFIED IBUPROFEN IBUPROFEN MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE 123 IBUPROFEN IBUPROFEN CROSCARMELLOSE SODIUM MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE POLYETHYLENE GLYCOL, UNSPECIFIED TALC TITANIUM DIOXIDE SILICON DIOXIDE IBUPROFEN IBUPROFEN STARCH, CORN POLYVINYL ALCOHOL, UNSPECIFIED 122

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
231 266 hi hjshdkshfkj 67836482764 yugthgistueg yugthgistueg 72189-231-90 72189-231-60 72189-231-30 72189-266-15

Spl medguide

Information about the patient medication guide that accompanies the drug product. Certain drugs must be dispensed with an accompanying medication guide. This field may contain information about when to consult the medication guide and the contents of the medication guide.
[MEDGUIDE IBUPROFEN TABLETS]

How supplied

Information about the available dosage forms to which the labeling applies, and for which the manufacturer or distributor is responsible. This field ordinarily includes the strength of the dosage form (in metric units), the units in which the dosage form is available for prescribing, appropriate information to facilitate identification of the dosage forms (such as shape, color, coating, scoring, and National Drug Code), and special handling and storage condition information.
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 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)

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API