Image-1 (449d2ef9 3580 46c8 8fe5 5d81cb18e40f 01)
Levothyroxine Sodium Tablet
Product Images NDC 51655-528
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Levothyroxine Sodium (NDC 51655-528). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Northwind Health Company, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Label 2 (51655 479 52 Master Bottle Label Approval Rev A 02 21)
NDC 51655-479-52 A is a prescription medicine containing Levothyroxine Sodium Tablets, USP. It comes in 150mcg (0.15mg) dose and is packed in a container of 30 tablets. The medication should be stored at 20°C to 25°C (68°F to 77°F) with excursions allowed from 15°C to 30°C (59°F to 86°F). It must be kept out of children's reach, protected from light and moisture in the original container. Each tablet consists of Levothyroxine Sodium USP 150 mcg (0.15mg). This medicine has been repackaged by Northwind Pharmaceuticals from Lupin Pharmaceuticals, Inc. (Lot: Indianapolis, IN 46203, Repackaged From: 68180-973-01). The S/N is 000000000000000. However, the expiration date of this medicine, as indicated by the EXP is 00/00/0000, and the LOT number is 0000000000.*
Label 2 (51655 528 52 Master Bottle Label Approval Rev A 01 21)
These are Levothyroxine Sodium Tablets USP, with 175mcg (0.175mg) strength, packed by Northwind Pharmaceuticals after repackaging from the original manufacturer, Lupin Pharmaceuticals. The tablets come in a pack of 30 that should be stored at room temperature, away from light and moisture. The product's safety profile and administration guidelines are included in the package insert. Access to the tablets should be restricted to keep out of the reach of children. The product has a unique identification code of NDC: 51655-528-52 and GTIN: 00351655528525. While the serial number, expiration date, and lot number of the product are 000000000000000, 00/00/0000, and 0000000000, respectively. This product is available only through a doctor's prescription.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
