Levothyroxine Sodium Tablet
Product Images NDC 0378-1819

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Levothyroxine Sodium (NDC 0378-1819). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Pharmaceuticals 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.

FDA Label Image

Levothyroxine Sodium Tablets, Usp 25 Mcg Bottle Label (Image 01)

Label for Levothyroxine Sodium Tablets, USP 25 mcg (0.025 mg) by Mylan Pharmaceuticals Inc., containing 90 oral tablets. The label includes dosage details, storage instructions, manufacturer information, a barcode, and a visual of the peach-colored tablet. It specifies dispensing in a child-resistant container and mentions lot and expiration printing details.*

FDA Label Image

Levothyroxine Sodium Tablets, Usp 50 Mcg Bottle Label (Image 02)

Label for Levothyroxine Sodium Tablets, USP 50 mcg (0.05 mg) by Mylan Pharmaceuticals Inc. The label shows the drug name, strength, dosage form, national drug code (NDC 0378-1803-77), and quantity of 90 tablets. It includes storage instructions, manufacturer details, and barcode. The label also notes the requirement for a child-resistant container and variable data coding areas for lot and expiration information.*

FDA Label Image

Levothyroxine Sodium Tablets, Usp 75 Mcg Bottle Label (Image 03)

Label for Levothyroxine Sodium Tablets, USP 75 mcg (0.075 mg) by Mylan Pharmaceuticals Inc. The label indicates the product contains 90 oral tablets, is prescription only, and instructs storage at 20° to 25°C with protection from light and moisture. The package includes NDC 0378-1805-77 and notes manufacturing in India for Mylan in Morgantown, WV.*

FDA Label Image

Levothyroxine Sodium Tablets, Usp 88 Mcg Bottle Label (Image 04)

Packaging label for Levothyroxine Sodium Tablets, USP 88 mcg (0.088 mg) by Mylan Pharmaceuticals Inc. The label shows the NDC 0378-1807-77, tablet strength, quantity of 90 tablets, and contains storage instructions, manufacturer information, and a barcode. It also includes warnings to keep the medication out of children's reach and to store at 20° to 25°C.*

FDA Label Image

Levothyroxine Sodium Tablets, Usp 100 Mcg Bottle Label (Image 05)

Label for Levothyroxine Sodium Tablets, USP 100 mcg (0.1 mg) by Mylan Pharmaceuticals Inc. The label shows the product name, strength, dosage form, and quantity of 90 tablets. It includes usage, storage instructions, manufacturing details (Made in India), a barcode, and child-resistant container warnings.*

FDA Label Image

Levothyroxine Sodium Tablets, Usp 112 Mcg Bottle Label (Image 06)

Label for Levothyroxine Sodium tablets, USP, 112 mcg (0.112 mg), oral tablets. The label includes dosage strength, manufacturer Mylan Pharmaceuticals Inc., storage instructions, NDC 0378-1811-77, barcode, and package size of 90 tablets. It features warnings to keep out of reach of children and protect from light and moisture. Variable data coding area marked for lot and expiration information.*

FDA Label Image

Levothyroxine Sodium Tablets, Usp 125 Mcg Bottle Label (Image 07)

Levothyroxine Sodium 125 mcg (0.125 mg) oral tablets packaging label from Mylan Pharmaceuticals Inc. The label indicates the product contains 90 tablets, with safety and storage instructions, including keeping out of reach of children and storage at 20° to 25°C. The label also displays the NDC number 0378-1813-77, barcode, and tablet imprint 'L 10', with information on dispensing and container specifications.*

FDA Label Image

Levothyroxine Sodium Tablets, Usp 137 Mcg Bottle Label (Image 08)

Label for Levothyroxine Sodium Tablets, USP 137 mcg (0.137 mg) by Mylan Pharmaceuticals Inc. The label shows 90 tablets in the package and includes instructions on dosage, storage temperature (20° to 25°C), and child-resistant container use. It features a barcode, NDC 0378-1823-77, and notes the product is manufactured in India for Mylan in West Virginia, USA.*

FDA Label Image

Levothyroxine Sodium Tablets, Usp 150 Mcg Bottle Label (Image 09)

Label for Levothyroxine Sodium 150 mcg (0.15 mg) tablets by Mylan Pharmaceuticals Inc. The label states 'Tablets, USP' with a count of 90 tablets. It includes storage instructions, dosage warnings, manufacturer information, a bar code, and a note on tight container use and variable data coding for lot and expiration details.*

FDA Label Image

Levothyroxine Sodium Tablets, Usp 175 Mcg Bottle Label (Image 10)

Levothyroxine Sodium 175 mcg (0.175 mg) oral tablets, USP, manufactured for Mylan Pharmaceuticals Inc. The label shows a purple tablet marked with 'L' and '12', with a quantity of 90 tablets per bottle. It includes dosage and storage instructions, a barcode, and a space for variable data coding including lot number and expiration date.*

FDA Label Image

Levothyroxine Sodium Tablets, Usp 200 Mcg Bottle Label (Image 11)

Levothyroxine Sodium 200 mcg (0.2 mg) Tablets, USP label for oral use by Mylan Pharmaceuticals Inc. The label indicates a 90-tablet bottle. It includes storage instructions, dosage information, and packaging details such as a barcode and lot/expiration date area for variable data coding.*

FDA Label Image

Levothyroxine Sodium Tablets, Usp 300 Mcg Bottle Label (Image 12)

Levothyroxine Sodium Tablets, USP 300 mcg (0.3 mg) oral tablets in a 90-tablet package by Mylan Pharmaceuticals Inc. The label includes storage instructions, active ingredient and strength, manufacturer details, NDC 0378-1821-77, barcode, and usage directions for a child-resistant container.*

FDA Label Image

Levothyroxine Sodium Structural Formula (Image 13)

Chemical structure diagram of levothyroxine sodium, showing the molecular arrangement including iodine atoms, hydroxyl group, amino group, carboxylate group, and water of hydration component.*

* 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.