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| Product NDC Code | 71335-1396 | ||||||||||||||||||||||
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| Drug Name | Ibuprofen |
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| Type | Generic | ||||||||||||||||||||||
| Pharm Class | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
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| Active Ingredients |
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| Route | ORAL | ||||||||||||||||||||||
| Dosage Form | TABLET, FILM COATED | ||||||||||||||||||||||
| RxCUI drug identifier | 197805, 197806, 197807 |
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| Application Number | ANDA090796 | ||||||||||||||||||||||
| Labeler Name | Bryant Ranch Prepack | ||||||||||||||||||||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Spl product data elements
Usually a list of ingredients in a drug product.IBUPROFEN IBUPROFEN SILICON DIOXIDE CROSCARMELLOSE SODIUM MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POLYETHYLENE GLYCOL, UNSPECIFIED POLYVINYL ALCOHOL, UNSPECIFIED STARCH, CORN TALC TITANIUM DIOXIDE IBUPROFEN IBUPROFEN 123 IBUPROFEN IBUPROFEN SILICON DIOXIDE CROSCARMELLOSE SODIUM MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POLYETHYLENE GLYCOL, UNSPECIFIED POLYVINYL ALCOHOL, UNSPECIFIED STARCH, CORN TALC TITANIUM DIOXIDE IBUPROFEN IBUPROFEN 122 IBUPROFEN IBUPROFEN SILICON DIOXIDE CROSCARMELLOSE SODIUM MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POLYETHYLENE GLYCOL, UNSPECIFIED POLYVINYL ALCOHOL, UNSPECIFIED STARCH, CORN TALC TITANIUM DIOXIDE IBUPROFEN IBUPROFEN 121
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.Ibuprofen 800mg Tablet Label Image
Ibuprofen 600mg Tablet Label Image
Ibuprofen 400mg Tablet Label Image
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.ibuprofen tablets 400 mg - 600 mg- 800 mg medguide 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.HOW SUPPLIED Product: 71335-1396 NDC: 71335-1396-0 84 TABLET, FILM COATED in a BOTTLE NDC: 71335-1396-1 20 TABLET, FILM COATED in a BOTTLE NDC: 71335-1396-2 15 TABLET, FILM COATED in a BOTTLE NDC: 71335-1396-3 40 TABLET, FILM COATED in a BOTTLE NDC: 71335-1396-4 21 TABLET, FILM COATED in a BOTTLE NDC: 71335-1396-5 30 TABLET, FILM COATED in a BOTTLE NDC: 71335-1396-6 90 TABLET, FILM COATED in a BOTTLE NDC: 71335-1396-7 100 TABLET, FILM COATED in a BOTTLE NDC: 71335-1396-8 120 TABLET, FILM COATED in a BOTTLE NDC: 71335-1396-9 60 TABLET, FILM COATED in a BOTTLE Product: 71335-1503 NDC: 71335-1503-0 21 TABLET, FILM COATED in a BOTTLE NDC: 71335-1503-1 20 TABLET, FILM COATED in a BOTTLE NDC: 71335-1503-2 15 TABLET, FILM COATED in a BOTTLE NDC: 71335-1503-3 30 TABLET, FILM COATED in a BOTTLE NDC: 71335-1503-4 40 TABLET, FILM COATED in a BOTTLE NDC: 71335-1503-5 60 TABLET, FILM COATED in a BOTTLE NDC: 71335-1503-6 90 TABLET, FILM COATED in a BOTTLE NDC: 71335-1503-7 120 TABLET, FILM COATED in a BOTTLE NDC: 71335-1503-8 50 TABLET, FILM COATED in a BOTTLE NDC: 71335-1503-9 100 TABLET, FILM COATED in a BOTTLE Product: 71335-1517 NDC: 71335-1517-1 20 TABLET, FILM COATED in a BOTTLE NDC: 71335-1517-2 30 TABLET, FILM COATED in a BOTTLE NDC: 71335-1517-3 40 TABLET, FILM COATED in a BOTTLE NDC: 71335-1517-4 60 TABLET, FILM COATED in a BOTTLE NDC: 71335-1517-5 90 TABLET, FILM COATED in a BOTTLE NDC: 71335-1517-6 120 TABLET, FILM COATED in a BOTTLE NDC: 71335-1517-7 100 TABLET, FILM COATED in a BOTTLE NDC: 71335-1517-8 21 TABLET, FILM COATED in a BOTTLE NDC: 71335-1517-9 15 TABLET, FILM COATED in a BOTTLE
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