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| Product NDC Code | 70771-1110 | ||||||
|---|---|---|---|---|---|---|---|
| Drug Name | Mesalamine |
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| Type | Generic | ||||||
| Pharm Class | Aminosalicylate [EPC], Aminosalicylic Acids [CS] |
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| Active Ingredients |
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| Route | ORAL | ||||||
| Dosage Form | TABLET, DELAYED RELEASE | ||||||
| RxCUI drug identifier | 833234 | ||||||
| Application Number | ANDA203286 | ||||||
| Labeler Name | Zydus Lifesciences Limited | ||||||
| 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.mesalamine mesalamine MESALAMINE MESALAMINE ACETYLTRIBUTYL CITRATE SILICON DIOXIDE FERRIC OXIDE RED MAGNESIUM STEARATE METHACRYLIC ACID CELLULOSE, MICROCRYSTALLINE POVIDONE SODIUM STARCH GLYCOLATE TYPE A POTATO TALC TITANIUM DIOXIDE FERROSOFERRIC OXIDE ISOPROPYL ALCOHOL BUTYL ALCOHOL PROPYLENE GLYCOL AMMONIA SHELLAC REDDISH-BROWN CAPSULE 435
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.PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1110-8 in bottle of 180 tablets Mesalamine Delayed-release Tablets USP, 800 mg R x only 180 tablets Mesalamine Delayed-release Tablets USP, 800 mg
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