Sign In

Save up to 80% by drug discount in your pharmacy with "Pharmacy Near Me - National Drug Discount Card"

You can scan QR Code(just open camera on your phone/scan by application) from the image on prescription drug discount card to save it to your mobile phone. Or just click on image if you're on mobile phone.

View Generic:
View Brand:

Ibuprofen - Medication Information

Product NDC Code 68071-3362
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 197807
Application Number ANDA090796
Labeler Name NuCare Pharmaceuticals,Inc.
Packages
Package NDC Code Description
68071-3362-0 12 tablet, film coated in 1 bottle (68071-3362-0)
68071-3362-1 21 tablet, film coated in 1 bottle (68071-3362-1)
68071-3362-2 20 tablet, film coated in 1 bottle (68071-3362-2)
68071-3362-3 30 tablet, film coated in 1 bottle (68071-3362-3)
68071-3362-4 40 tablet, film coated in 1 bottle (68071-3362-4)
68071-3362-5 15 tablet, film coated in 1 bottle (68071-3362-5)
68071-3362-6 60 tablet, film coated in 1 bottle (68071-3362-6)
68071-3362-9 90 tablet, film coated in 1 bottle (68071-3362-9)
Check if available Online

Spl product data elements

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

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.
800mg Ibuprofen Package Label PDP

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.
HOW SUPPLIED NDC 68071-3362-0 Bottles of 12 NDC 68071-3362-5 Bottles of 15 NDC 68071-3362-2 Bottles of 20 NDC 68071-3362-1 Bottles of 21 NDC 68071-3362-3 Bottles of 30 NDC 68071-3362-4 Bottles of 40 NDC 68071-3362-6 Bottles of 60 NDC 68071-3362-9 Bottles of 90

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