Levothyroxine Sodium Tablet
Product Images NDC 0527-3288

Product Visual Gallery

This gallery contains 25 technical images submitted to the FDA as part of the official labeling for Levothyroxine Sodium (NDC 0527-3288). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lannett Company, 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

100 Mcg 1000s (Levo 100 Mcg 1000s)

Label for Levothyroxine Sodium Tablets, USP 100 mcg (0.1 mg), oral tablet. The label indicates Rx only, with a count of 1000 tablets. It includes storage instructions to keep at 25°C (77°F) with permitted excursions, protection from light and moisture, and dispensing in a child-resistant container. Manufactured by Neolpharma, Inc. and distributed by Lannett Company, Inc.*

FDA Label Image

100 Mcg 90s (Levo 100 Mcg 90s)

Label for Levothyroxine Sodium Tablets, USP 100 mcg (0.1 mg) oral tablets by Lannett Company, Inc. The label indicates 90 tablets per container, Rx only. Storage instructions specify 25°C with allowable excursions and light protection. Additional product and manufacturing details are provided on the label.*

FDA Label Image

112 Mcg 1000s (Levo 112 Mcg 1000s)

Label for Levothyroxine Sodium Tablets, USP 112 mcg (0.112 mg) manufactured by Neolpharma, Inc. and distributed by Lannett Company, Inc. The label includes storage instructions, usual dosage information, and indicates a package size of 1000 tablets. The NDC number is 0527-3285-43, and the product is marked Rx only.*

FDA Label Image

112 Mcg 90s (Levo 112 Mcg 90s)

Label for Levothyroxine Sodium Tablets USP 112 mcg (0.112 mg) by Lannett Company, Inc. The oral tablet packaging indicates 'Rx Only' and contains 90 tablets. Storage instructions and usual dosage range (100 to 200 mcg daily) are included, along with package barcode and lot/issue information.*

FDA Label Image

125 Mcg 1000s (Levo 125 Mcg 1000s)

Label for Levothyroxine Sodium Tablets USP 125 mcg (0.125 mg) by Lannett Company, Inc. The label includes dosage instructions, storage conditions, barcode, and note that the product contains 1000 tablets for prescription use only. Manufactured by Neolpharma, Inc., Puerto Rico, and distributed by Lannett Company, Philadelphia, PA.*

FDA Label Image

125 Mcg 90s (Levo 125 Mcg 90s)

Levothyroxine Sodium Tablets, USP 125 mcg (0.125 mg) oral tablets, labeled by Lannett Company, Inc. The label indicates a package containing 90 tablets with prescription use only. Storage instructions advise protection from light and moisture, with storage temperatures specified. The label includes a barcode and lot information.*

FDA Label Image

137 Mcg 1000s (Levo 137 Mcg 1000s)

Label for Levothyroxine Sodium Tablets USP, 137 mcg (0.137 mg) strength, oral tablets. The label includes storage instructions, dosage range, manufacturer Neolpharma, Inc., distributor Lannett Company, Inc., and specifies 1000 tablets in the container. NDC number 0527-3287-43 is visible with barcode and batch information.*

FDA Label Image

137 Mcg 90s (Levo 137 Mcg 90s)

Label for Levothyroxine Sodium Tablets USP, 137 mcg (0.137 mg) strength. The label indicates the product is an oral tablet manufactured by Lannett Company, Inc. It includes dosage instructions mentioning 100 to 200 mcg daily and storage conditions. The package contains 90 tablets and is marked Rx Only.*

FDA Label Image

150 Mcg 1000s (Levo 150 Mcg 1000s)

Label for Levothyroxine Sodium Tablets, USP, 150 mcg (0.150 mg) strength. The label shows the product name, strength, dosage form, quantity of 1000 tablets, and is marked Rx Only. It includes storage instructions and manufacturer information: Neolpharma, Inc., distributed by Lannett Company, Inc.*

FDA Label Image

150 Mcg 90s (Levo 150 Mcg 90s)

Label for Levothyroxine Sodium Tablets USP 150 mcg (0.150 mg), oral tablets, in a 90-tablet bottle. The label includes dosage storage instructions, the product NDC 0527-3288-46, the Rx only designation, and identifies Lannett Company, Inc. as the distributor with packaging information indicating it is manufactured by Neolpharma, Inc.*

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175 Mcg 1000s (Levo 175 Mcg 1000s)

Label for Levothyroxine Sodium Tablets, USP 175 mcg (0.175 mg), oral tablets in a 1000 count package. The label includes storage instructions, usual dosage range, manufacturer Neopharma, Inc., and distributor Lannett Company, Inc. The product is prescription-only and the label shows an NDC number 0527-3289-43 with a barcode.*

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175 Mcg 90s (Levo 175 Mcg 90s)

Label for Levothyroxine Sodium Tablets, USP, strength 175 mcg (0.175 mg), oral tablets. The package contains 90 tablets and is labeled for prescription use only. The label includes dosage storage instructions and manufacturer details, showing Lannett Company, Inc as the labeler.*

FDA Label Image

200 Mcg 1000s (Levo 200 Mcg 1000s)

Label for Levothyroxine Sodium Tablets, USP 200 mcg (0.2 mg), oral tablets, packaged in a container of 1000 tablets. The label includes storage instructions and manufacturer information, showing Lannett Company, Inc. as the distributor and Neolpharma, Inc. as the manufacturer. The label features an NDC number 0527-3290-43 and a barcode.*

FDA Label Image

200 Mcg 90s (Levo 200 Mcg 90s)

Levothyroxine Sodium Tablets, USP 200 mcg (0.2 mg) oral tablets label by Lannett Company, Inc. The label shows a pack of 90 tablets with dosage and storage instructions. It is indicated as Rx only and includes the NDC 0527-3290-46.*

FDA Label Image

25 Mcg 1000s (Levo 25 Mcg 1000s)

Label for Levothyroxine Sodium Tablets, USP 25 mcg (0.025 mg) by Lannett Company, Inc. The bottle contains 1000 tablets for oral use. Storage instructions include maintaining at 25°C (77°F) with permitted excursions and protection from light and moisture. The label includes dosage guidance and distributor information.*

FDA Label Image

25 Mcg 90s (Levo 25 Mcg 90s)

Levothyroxine Sodium Tablets, USP 25 mcg (0.025 mg) oral tablets label showing the drug name, strength, and quantity of 90 tablets. The label includes usage directions, storage instructions, barcode, NDC 0527-3280-46, and manufacturer details from Lannett Company, Inc. The label states Rx Only and includes distribution information.*

FDA Label Image

300 Mcg 1000s (Levo 300 Mcg 1000s)

Label for Levothyroxine Sodium Tablets USP, 300 mcg (0.3 mg), oral tablets. The label includes storage instructions, usual dosage range, manufacturer Neolpharma, Inc., and distributor Lannett Company, Inc. The package contains 1000 tablets and is marked Rx Only. It features a barcode and lot/expiration date area.*

FDA Label Image

300 Mcg 90s (Levo 300 Mcg 90s)

Label of Levothyroxine Sodium Tablets, USP, 300 mcg (0.3 mg) strength, oral tablets packaged by Lannett Company, Inc. The label indicates storage instructions, usual dosage range of 100 to 200 mcg daily, Rx only, and contains 90 tablets per container. The label shows barcode information and distribution details by Lannett Company, Inc.*

FDA Label Image

50 Mcg 1000s (Levo 50 Mcg 1000s)

Label for Levothyroxine Sodium tablets, USP, 50 mcg (0.050 mg) strength, in a pack containing 1000 tablets. The label includes storage instructions to keep at 25°C (77°F) with permitted excursions from 15° to 30°C (59° to 86°F), and directions to protect from light and moisture in a child-resistant container. Manufactured by Neolpharma, Inc. and distributed by Lannett Company, Inc.*

FDA Label Image

50 Mcg 90s (Levo 50 Mcg 90s)

Label for Levothyroxine Sodium Tablets USP, 50 mcg (0.050 mg) dosage form. The label specifies 90 tablets per package, prescription use only (Rx Only), and includes storage instructions and distributor information. It is labeled by Lannett Company, Inc.*

FDA Label Image

75 Mcg 1000s (Levo 75 Mcg 1000s)

Label for Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg) strength. This prescription drug label shows a package size of 1000 tablets. It includes storage instructions to keep at 25°C (77°F) with permitted excursions between 15° to 30°C. The label indicates the product is manufactured by Neolpharma, Inc. and distributed by Lannett Company, Inc.*

FDA Label Image

75 Mcg 90s (Levo 75 Mcg 90s)

Label for Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg) oral tablets. The label includes dosage instructions, storage information, and manufacturer details for 90 tablets by Lannett Company, Inc. The label also features a barcode and NDC number 0527-3282-46.*

FDA Label Image

88 Mcg 1000s (Levo 88 Mcg 1000s)

Label for Levothyroxine Sodium Tablets, USP 88 mcg (0.088 mg) oral tablets. The label includes the NDC 0527-3283-43 and indicates the product is prescription only with a total count of 1000 tablets. It advises usual dosages from 100 to 200 mcg daily, with storage instructions at 25°C (77°F) and allowance for excursions from 15° to 30°C (59° to 86°F). The label lists Neolpharma, Inc. as the manufacturer and Lannett Company, Inc. as the distributor.*

FDA Label Image

88 Mcg 90s (Levo 88 Mcg 90s)

Label for Levothyroxine Sodium Tablets USP, 88 mcg (0.088 mg), oral tablets. The label indicates a package containing 90 tablets, manufactured by Neolpharma, Inc and distributed by Lannett Company, Inc. It includes dosage instructions, storage conditions at 25°C with temperature excursions allowed, and mentions dispensing in light-resistant containers with child-resistant closures. The label is marked Rx only and includes a barcode and NDC number 0527-3283-46.*

FDA Label Image

Levothyroixe Molecule (Levothyroxine Molecule)

Chemical structure of Levothyroxine Sodium, showing the molecule's iodine-substituted aromatic rings, amino group, carboxylate salt, and associated 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.