Cdld-structure-carbidopa (Cdld Structure Carbidopa)
Carbidopa And Levodopa Tablet
Product Images NDC 62756-985
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Carbidopa And Levodopa (NDC 62756-985). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Sun Pharmaceutical Industries, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Cdld-structure-levodopa (Cdld Structure Levodopa)
Spl Cdld 25 250mg Label2
Spl Cdld Label 1
This is a medication containing 10 mg of Carbidopa USP and 100 mg of Levodopa USP in tablet form. It is distributed by Sun Pharmaceutical Industries and manufactured in Gujarat, India. The recommended adult dosage and storage instructions are provided with the accompanying prescribing information. It should be kept in a tightly closed, light-resistant container and out of reach of children.*
Spl Cdld Label2
This text is a label for medication that contains both Carbidopa and Levodopa in various amounts. The usual adult dosage is not provided on the label, only an instruction to refer to the accompanying prescribing information. The medication should be stored in a tightly closed container at a temperature between 20°C to 25°C, and in a place protected from light and moisture. Dispensation should also be done in a tightly closed, light-resistant container. The label also includes a warning to keep the medication out of reach of children. The medication comes in a pack of 100 tablets, and the label provides additional information such as the NDC number, the manufacturer's name, and the place of distribution.*
Spl Cdld Label3
Carbidopa and Levodopa Tablets, USP, are a type of medication which come in 25 mg/250 mg strength. The usual adult dosage is not given and has to be obtained from the accompanying prescribing information. The tablets should be stored at between 20°-25°C (66°-77°F) in a tightly closed container, away from light and moisture, and should be dispensed in a tightly closed, light-resistant container. The medication should be kept out of the reach of children. The product is available in a package of 100 tablets with the NDC code 62756-519-88. The manufacturer and distributor of the product is Sun Pharmaceuticals Industries. The product package also contains a product code- PJLBO758D and a code- GUJ/DRUGS/25/789.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
