Levothyroxine Sodium Tablet
Product Images NDC 42292-038

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Levothyroxine Sodium (NDC 42292-038). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Institutional 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 112 Mcg (0.112 mg) Tablets Unit Carton Label (Image 01)

Label for Levothyroxine Sodium tablets, USP, 88 mcg (0.088 mg) oral tablets by Mylan Institutional Inc. The label displays the NDC 42292-038-20, the tablet strength, a depiction of the tablet imprint L17, and packaging information for 100 tablets (10 x 10). Storage instructions and usage notes are included.*

FDA Label Image

Image 02

Packaging label for Levothyroxine Sodium tablets by Mylan Institutional Inc., featuring bright blue background with UNIT-DOSE prominently displayed. The label includes safety instructions for unit dose packages, emphasizing it is not child resistant and for institutional use only. The distributor's information and lot number/expiration window are visible on the label.*

FDA Label Image

Levothyroxine Sodium 88 Mcg (0.088 mg) Tablets Unit Carton Label (Image 03)

Packaging label for Levothyroxine Sodium Tablets, USP, 112 mcg (0.112 mg) oral tablets. The label displays the strength prominently in orange with the generic name levothyroxine sodium. The package contains 100 tablets (10 x 10) and is labeled for prescription use only. The labeler is Mylan Institutional Inc.*

FDA Label Image

Unit Carton (Image 04)

Packaging label for Levothyroxine Sodium oral tablets distributed by Mylan Institutional Inc. The label features a blue background with the UNIT-DOSE designation, safety warnings indicating the unit dose package is not child resistant, and instructions for institutional use. The Mylan logo and distributor information are clearly displayed, along with a lot number and expiration window on the back.*

FDA Label Image

Image 05

Levothyroxine Sodium 137 mcg (0.137 mg) tablets, USP oral dosage form by Mylan Institutional Inc. The label includes dosage strength, NDC number 42292-041-20, barcode, quantity of 100 tablets (10 x 10), and storage instructions. The tablets are marked with 'L 15.'*

FDA Label Image

Unit Carton (Image 06)

The image shows a unit-dose packaging label for Levothyroxine Sodium tablets by Mylan Institutional Inc. The label is blue with white text and includes safety instructions stating that the package is not child-resistant and is for institutional use only. It advises keeping the product away from children and notes the container's light resistance. There is a window for lot number and expiration date, with a QR code and additional product identifiers on the back.*

FDA Label Image

Image 07

Label for Levothyroxine Sodium Tablets, USP, 175 mcg (0.175 mg) oral tablets by Mylan Institutional Inc. The label shows the NDC 42292-040-20 and indicates a package of 100 tablets (10 x 10). It includes the tablet imprint 'L 112' and states Rx only with dosage guidelines and storage conditions.*

FDA Label Image

Image 08

Packaging label for Levothyroxine Sodium oral tablets in unit-dose format from Mylan Institutional Inc. The blue label includes usage instructions, safety warnings, and a window for lot number and expiration date. It states the product is for institutional use and provides light resistance protection.*

FDA Label Image

Image 13

Chemical structure of levothyroxine sodium, showing two iodinated benzene rings connected by an ether linkage, with an amino acid side chain featuring sodium carboxylate and amino groups.*

* 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.