Fenofibrate Tablet
Product Images NDC 68180-388

This is a description of a medication product with the National Drug Code (NDC) 68180-388-09. The dosage information is not provided and can only be found in the prescribing information that accompanies the product. The medication is manufactured for Lupin Pharmaceuticals, Inc. in Baltimore, Maryland. The product should be kept in a tightly closed container away from children, stored at 25°C (77°F) and protected from moisture. The tablets contain 48 mg of fenofibrate USP, and there are 90 tablets in each bottle. The code number is MH/DRUGS/25-ND/59. The description also includes directions to not accept the product if the seal over the bottle opening is broken or missing.*

This is a description of medication with NDC code 68180-361-09, containing fenofibrate USP 145 mg per film-coated tablet. The dosage is not provided and must be found in accompanying prescribing information. The medication is manufactured by Lupin Pharmaceuticals Inc. and manufactured in Nagpur, India. It should be stored in a tightly closed container at 25°C (77°F) with excursions permitted to 15 to 30°C (59 to 86°F) and protected from moisture. The medication should not be accepted if the seal over the bottle opening is broken or missing. The label includes a "Code No. MH/DRUGS/25-ND/59". It is only available through prescription and must be kept out of the reach of children.*

This is a prescription drug called fenofibrate, which comes in a tablet form of 145mg. The tablets are manufactured by Lupin Pharmaceuticals and are to be kept in tightly closed containers at controlled room temperature, protected from moisture at 25°C (77°F) with excursions permitted. The text also includes the manufacturer's code and precautions for storage and handling.*