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Mesalamine - Medication Information

Product NDC Code 70771-1071
Drug Name

Mesalamine

Type Generic
Pharm Class Aminosalicylate [EPC],
Aminosalicylic Acids [CS]
Active Ingredients
Mesalamine 1.2 g/1
Route ORAL
Dosage Form TABLET, DELAYED RELEASE
RxCUI drug identifier 686429
Application Number ANDA091640
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
70771-1071-1 120 tablet, delayed release in 1 bottle (70771-1071-1)
70771-1071-2 34 tablet, delayed release in 1 bottle (70771-1071-2)
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Spl product data elements

Usually a list of ingredients in a drug product.
mesalamine mesalamine MESALAMINE MESALAMINE CARBOXYMETHYLCELLULOSE SODIUM CELLULOSE, MICROCRYSTALLINE FERRIC OXIDE RED FERRIC OXIDE YELLOW HYPROMELLOSES MAGNESIUM STEARATE METHACRYLIC ACID POLYETHYLENE GLYCOL, UNSPECIFIED SILICON DIOXIDE SODIUM STARCH GLYCOLATE TYPE A POTATO TALC TITANIUM DIOXIDE TRIETHYL CITRATE BROWN OVAL 711

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 70771-1071-1 Mesalamine Delayed-release Tablets, 1.2 g Rx only 120 tablets Mesalamine DR Tablets, 1.2 g

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