Levothyroxine Sodium Tablet
Product Images NDC 0904-6951

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Levothyroxine Sodium (NDC 0904-6951). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major Pharmaceuticals, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

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FDA Label Image

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This is a description for a medication called Levothyroxine in tablet form. The medication is manufactured by a company named Major. The medication comes in a bottle containing 100 unit dose tablets. The national drug code (NDC) for the medication is 0904-6957-61. The medication is only available with a prescription. The package is designed to keep the medicine out of the reach of children.*

FDA Label Image

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This is a description of a medication package containing unit dose tablets of Levothyroxine Sodium in 150 mcg strength. It is prescribed for restricted use and is labeled for prescription-only. The Universal Product Code (UPC) of the product is 0904-6956-61 and manufactured by MAJOR Pharmaceuticals.*

FDA Label Image

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This text describes a medication called Levothyroxine Sodium Tablets USP with a strength of 100 mcg (0.1 mg) and comes in a unit dose package. It is used only with a prescription and the package should be kept away from reach. The NDC number is provided as 0904695361.*

FDA Label Image

Carton Label (Image 01)

FDA Label Image

Carton Label (Image 02)

This is a description of a medication called Levothyroxine Sodium Tablets USP. The tablets come in 50 mcg (0.05 mg) strength and are available in unit dose packaging. The medicine can only be obtained with a prescription. The text also includes the National Drug Code (NDC) number for the medication.*

FDA Label Image

Carton Label (Image 03)

This is a unit dose package of Levothyroxine Sodium Tablets USP from MAJOR Pharmaceuticals. The package contains 100 tablets, each with 75 mcg (0.075 mg) of Levothyroxine Sodium USP. This medication is only available through prescription and should be stored between 25°C (77°F) and 30°C (86°F). The package is not child-resistant and is intended for institutional use only. The product insert or prescribing information should be consulted for dosage, precautions, and warnings. For more information, see the insert found at the manufacturer's website.*

FDA Label Image

Carton Label (Image 04)

This is a medication package of Levothyroxine Sodium tablets, USP with a dosage strength of 88 mcg (0.088mg) which contains 100 tablets. It is a prescription-only medication and the NDC code of the package is 0904-6952-61. The package is designed as a unit dose. The last few lines of text are not readable due to poor quality.*

FDA Label Image

Carton Label (Image 05)

This is a prescription medication, Levothyroxine Sodium Tablets USP, with a strength of 112 mcg (0.112 mg). Each tablet contains Levothyroxine Sodium USP 112 mcg (0.112 mg). The usual dosage and precautions should be followed as per the product insert or prescribing information. This medication should be stored at 25°C (77°F), protected from light and moisture in a tightly sealed, child-resistant container. This is a unit dose package intended for institutional use only. The distributor of this medication is Major Pharmaceuticals in the United States.*

FDA Label Image

Carton Label (Image 06)

This is a description of a medication called Levothyroxine Sodium Tablets. The tablets are 125 mcg (0.125 mg) and come in a unit dose package of 100 tablets. It is a prescription medication and should be kept in a light-resistant container between 25°C and 30°C. The manufacturer is Major and the product insert should be consulted for prescribing information and warnings. The NDC number is 0904-6955-61. This package is not child-resistant and is intended for institutional use only.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.