Levothyroxine Sodium
Product Images NDC 70934-292

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Levothyroxine Sodium (NDC 70934-292). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Denton Pharma, Inc. Dba Northwind Pharmaceuticals, 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

Label 25 (70934 266 30 Rev A 02 19)

Container label for Levothyroxine Sodium Tablets USP 25 mcg (0.025 mg), containing 30 tablets. The label includes storage instructions, NDC 70934-266-30, and designation as Rx only. It is labeled by Denton Pharma, Inc. DBA Northwind Pharmaceuticals.*

FDA Label Image

Label 50 (70934 273 30 Rev A 02 19)

Levothyroxine Sodium Tablets, USP 50 mcg (0.050 mg) in a package of 30 tablets. The label includes the NDC 70934-273-30, specifies prescription use only, and states storage instructions to keep the product between 15°C and 30°C (59°F and 86°F). The labeler is Denton Pharma, Inc. DBA Northwind Pharmaceuticals. Manufacturing and expiration details are present but not fully legible.*

FDA Label Image

Label 112 (70934 274 30 Rev A 02 19)

Levothyroxine Sodium Tablets, USP 112 mcg (0.112 mg), 30 tablets, packaged by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The label includes NDC 70934-274-30 and indicates the product is for prescription use only. Storage instructions and other regulatory information are also present.*

FDA Label Image

Label 75 (70934 292 30 Rev A 02 19)

Levothyroxine Sodium Tablets, USP 75 mcg (0.075 mg), package containing 30 tablets. The label includes storage instructions to keep at 20-25°C (68-77°F) with permitted excursions from 15-30°C (59-86°F), and advises to see the package insert for dosage. The product is marked as Rx Only and is labeled by Denton Pharma, Inc. DBA Northwind Pharmaceuticals.*

FDA Label Image

Label 100 (70934 308 30 Rev A 03 19)

Levothyroxine Sodium Tablets, USP 100 mcg (0.1 mg), 30 tablets per bottle, label by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The label indicates prescription use only with storage instructions between 20°-25°C and warnings to keep out of reach of children. The label features NDC 70934-308-30 and batch information.*

FDA Label Image

Label 150 (70934 314 30 Rev A 03 19)

Levothyroxine Sodium Tablets, USP 150 mcg (0.150 mg), package containing 30 tablets from Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The label includes dosage strength, quantity, storage instructions, and expiration and manufacturing details.*

FDA Label Image

Label 88 (70934 326 30 Rev A 04 19)

The image shows a white and orange rectangular packaging label for Levothyroxine Sodium Tablets, USP 88 mcg (0.088 mg) from Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The label indicates a count of 30 tablets, with storage instructions and warnings such as Rx only and excipients information. Multiple barcode and NDC numbers (70934-326-30) are also present.*

FDA Label Image

Chemical Structure (Levothyroxine Sodium Tablet Usp Jsp 1)

Chemical structure diagram of levothyroxine sodium showing the molecular arrangement including aromatic rings, hydroxyl groups, and sodium salt with hydrate notation.*

* 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.