Levothyroxine Sodium Tablet
Product Images NDC 51079-445

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Levothyroxine Sodium (NDC 51079-445). 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 25 Mcg (0.025 mg) Tablets Unit Carton Label (Image 01)

Levothyroxine Sodium 25 mcg (0.025 mg) oral tablets, USP, shown in a peach, film-coated, oval-shaped tablet with imprint 'L 4'. The package contains 100 tablets (10 x 10) and is labeled by Mylan Pharmaceuticals Inc. with instructions to store at 20° to 25°C and protect from light and moisture. This is a human prescription drug.*

FDA Label Image

Levothyroxine Sodium 50 Mcg (0.05 mg) Tablets Unit Carton Label (Image 02)

Packaging label for Levothyroxine Sodium oral tablets in unit-dose packaging by Mylan Institutional Inc. The label is blue with white text, indicating institutional use, child safety warnings, and light-resistant container features. It includes Mylan's logo and distribution address in Rockford, Illinois, with a barcode and lot/expiration date window.*

FDA Label Image

Image 03

Label for Levothyroxine Sodium Tablets, USP 50 mcg (0.05 mg) from Mylan Institutional Inc. The label features the drug name and strength in green text, with an image of a round white tablet marked L and 5. It indicates a package size of 100 tablets and includes prescribing information highlights and storage instructions from Mylan Pharmaceuticals Inc.*

FDA Label Image

Image 04

Packaging label for Levothyroxine Sodium unit-dose tablet by Mylan Institutional Inc. The blue packaging displays instructions indicating it is for institutional use only, not child resistant, and provides light resistance. It includes a visible window for lot number and expiration date.*

FDA Label Image

Levothyroxine Sodium 10 Mcg (0.1 mg) Tablets Unit Carton Label (Image 05)

The image shows a packaging label for Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg) oral tablets. The label includes the NDC 51079-441-20 and depicts a round tablet imprinted with 'L 6'. It states the quantity as 100 tablets, provided as 10 blister packs of 10 tablets each. The label is from Mylan Pharmaceuticals Inc., Morgantown, WV, with manufacturing noted in India. Additional storage information and usage references are included.*

FDA Label Image

Image 06

Blue unit-dose packaging labeled for Levothyroxine Sodium tablets distributed by Mylan Institutional Inc. The front displays usage and safety instructions including light-resistance and institutional use, along with a company logo and address. The back features a white label with a QR code and placeholders for NDC, expiration, and lot number information.*

FDA Label Image

Levothyroxine Sodium 125 Mcg (0.125 mg) Tablets Unit Carton Label (Image 07)

Levothyroxine Sodium Tablets, USP 100 mcg (0.1 mg) oral tablets, packaged in a box of 100 tablets (10 x 10) by Mylan Pharmaceuticals Inc. The label shows the NDC 51079-442-20, with dosage and storage instructions, and barcodes on a white background.*

FDA Label Image

Unit Carton (Image 08)

Packaging label for Levothyroxine Sodium oral tablets in unit-dose format. The label is predominantly blue and includes the Mylan Institutional Inc. logo and distributor information. It features cautionary notes about institutional use, child resistance, and storage, as well as a window for lot number and expiration date details.*

FDA Label Image

Levothyroxine Sodium 150 Mcg (0.15 mg) Tablets Unit Carton Label (Image 09)

Levothyroxine Sodium Tablets, USP 125 mcg (0.125 mg) in oral tablet form. The label shows the NDC 51079-443-20 and identifies the product as prescription-only. The package contains 100 tablets (10 x 10) and includes manufacturer information from Mylan Pharmaceuticals Inc., Morgantown, WV. The label includes storage instructions and tablet imprint details (L 10).*

FDA Label Image

Unit Carton (Image 10)

Packaging label for Levothyroxine Sodium oral tablets by Mylan Institutional Inc. The unit-dose package is blue and displays instructions noting it is not child resistant, for institutional use only, and provides light resistance. The label includes a window for the lot number and expiration date, with distribution details by Mylan Institutional Inc., Rockford, IL. A separate side of the package shows a QR code and printed lot and expiration information.*

FDA Label Image

Unit Carton (Image 11)

Label for Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg) strength. The label includes NDC 51079-445-20, bar code, quantity of 100 tablets (10 x 10), prescription use designation, storage instructions, patent information, and manufacturer details indicating Mylan Pharmaceuticals Inc. as the labeler.*

FDA Label Image

Levothyroxine Sodium 75 Mcg (0.075 mg) Tablets Unit Carton Label (Image 12)

Blue unit-dose packaging label for Levothyroxine Sodium tablets, distributed by Mylan Institutional Inc. The label includes instructions noting the package is not child resistant and is for institutional use only. It also highlights light-resistance of the container and advises keeping drugs out of children's reach. The label features a window area for lot number and expiration date, along with a printed QR code and product information on the reverse.*

FDA Label Image

Unit Carton (Image 13)

Chemical structure of levothyroxine sodium, showing two iodine-substituted phenyl rings connected by an ether linkage, and an amino acid side chain with an amino group and carboxylate ion, indicating the sodium salt form with hydration.*

* 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.