Levo-t
Product Images NDC 55466-107

Product Visual Gallery

This gallery contains 18 technical images submitted to the FDA as part of the official labeling for Levo-t (NDC 55466-107). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Neolpharma, 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

Levo T 100 Mcg 90s 6 5 18

LEVO-T (Levothyroxine Sodium Tablets, USP) label featuring strength of 100 mcg (0.1 mg). The label indicates a quantity of 90 tablets and is labeled for prescription use only (Rx only). The labeler is Neolpharma, Inc.*

FDA Label Image

Levo T 112 Mcg 90s 6 5 18

LEVO-T Levoothyroxine Sodium Tablets USP 112 mcg (0.112 mg) label showing 80 tablets in package. The label includes the proprietary name LEVO-T, strength, quantity, and the labeler Neolpharma, Inc. Barcode and NDC number are also visible.*

FDA Label Image

Levo T 125 Mcg 90s 6 5 18

LEVO-T (Levothyroxine Sodium) Tablets, USP, 125 mcg (0.125 mg) strength, displayed on a white box label. The package contains 80 tablets and is labeled for prescription use only. The label shows the Neolpharma, Inc. logo and includes an NDC number.*

FDA Label Image

Levo T 137 Mcg 90s 6 5 18

LEVO-T (Levothyroxine Sodium Tablets, USP) 137 mcg (0.137 mg) label showing a bottle containing 90 tablets. The label includes the product name, strength, dosage form, quantity, prescription-only status, and is labeled by Neolpharma, Inc. A barcode and NDC number 55466-111-11 are also visible.*

FDA Label Image

Levo T 150 Mcg 90s 6 5 18

LEVO-T (Levothyroxine Sodium Tablets, USP) 150 mcg (0.150 mg) tablet bottle label. The container holds 90 tablets and is labeled Rx only. The labeler is Neolpharma, Inc. The label includes the product name, active ingredient, strength, quantity, and barcodes.*

FDA Label Image

Levo T 175 Mcg 90s 6 5 18

Label for LEVO-T Levothyroxine Sodium Tablets, USP, showing strength of 175 mcg (0.175 mg). The label indicates the package contains 90 tablets and is for prescription use only. It displays the labeler name Neolpharma, Inc., along with the NDC number and barcode.*

FDA Label Image

Levo T 200 Mcg 90s 5 30 18

LEVO-T (Levo­thyroxine Sodium) Tablets, USP 200 mcg (0.2 mg) in a package of 90 tablets. The label shows the brand name LEVO-T prominently, with the active ingredient and strength below. The product is labeled for prescription use only and manufactured by Neolpharma, Inc. A UPC barcode is also visible.*

FDA Label Image

Levo T 25 Mcg 90s 6 5 18

LEVO-T Levofloxacin Sodium Tablets, USP label showing 25 mcg (0.025 mg) strength, containing 80 tablets. The label includes the Neolpharma, Inc. logo and barcode, specifying it is for prescription use only.*

FDA Label Image

Levo T 300 Mcg 90s 6 5 18

LEVO-T (Levothyroxine Sodium Tablets, USP) 300 mcg (0.3 mg) package label. The label displays the brand name LEVO-T prominently with dosage strength and form. It indicates a count of 90 tablets and specifies prescription use only. The label also features the manufacturer name Neolpharma, Inc.*

FDA Label Image

Levo T 50 Mcg 90s 6 5 18

The packaging label for LEVO-T (Levothyroxine Sodium Tablets, USP) by Neolpharma, Inc. Features the product name, active ingredient, and strength of 50 mcg (0.05 mg). The label indicates a count of 80 tablets and specifies that the product is prescription only. Includes barcodes and trademark details.*

FDA Label Image

Levo T 75 Mcg 90s 6 5 18

LEVO-T Levofloxacin Sodium Tablets USP 75 mcg (0.075 mg) label from Neolpharma, Inc. The label indicates a package size of 90 tablets and includes a barcode, along with usage instructions stating 'Rx only.' The Neolpharma logo is displayed at the bottom.*

FDA Label Image

Levo T 88 Mcg 90s 6 5 18

Packaging label for LEVO-T (Levothyroxine Sodium Tablets, USP) showing strength as 88 mcg (0.088 mg). The label indicates 90 tablets per bottle, prescription only, and is labeled by Neolpharma, Inc. A barcode and NDC 55466-107-11 are also visible.*

FDA Label Image

Levo Molecule (Levo Molecule)

Chemical structure diagram of the active ingredient in LEVO-T by Neolpharma, Inc., showing a molecule with iodine-substituted aromatic rings, a hydroxyl group, and an amino acid component labeled with sodium and variable hydration.*

FDA Label Image

Levo T 100 Mcg 1000s

LEVO-T (Levothyroxine Sodium Tablets, USP) 100 mcg (0.1 mg) package label displaying product name and strength. The label indicates a quantity of 1000 tablets and states 'Rx only'. The labeler is Neolpharma, Inc.*

FDA Label Image

Levo T 125 Mcg 1000s

LEVO-T (Levothyroxine Sodium Tablets, USP) 125 mcg (0.125 mg) tablet package label. The label indicates a quantity of 1000 tablets and lists Neolpharma, Inc. as the labeler. The product is marked as Rx only.*

FDA Label Image

Levo T 25 Mcg 1000s

LEVO-T 25 mcg (0.025 mg) tablets packaging label shows the active ingredient Levothyroxine Sodium, USP. The label indicates the quantity as 1000 tablets and is marked Rx only. The labeler is Neolpharma, Inc., with a logo at the bottom of the label.*

FDA Label Image

Levo T 50 Mcg 1000s

LEVO-T (Levothyroxine Sodium Tablets, USP) 50 mcg (0.05 mg) label showing a package of 1000 tablets. The label includes the brand name LEVO-T in large font, active ingredient Levothyroxine Sodium Tablets, the strength 50 mcg (0.05 mg), Rx only designation, and the labeler Neolpharma, Inc. logo.*

FDA Label Image

Levo T 75 Mcg 1000s

LEVO-T Levothyroxine Sodium Tablets, USP label showing strength of 75 mcg (0.075 mg). The label indicates a package quantity of 1000 tablets and is marked for prescription use only (Rx only). The labeler is Neolpharma, Inc.*

* 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.