Structural Formula (4b75b4c5 9511 4436 8a83 099f5e73f141 01)
Levothyroxine Sodium
Product Images NDC 53808-0679
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Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Levothyroxine Sodium (NDC 53808-0679). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by State Of Florida Doh Central Pharmacy, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Levothyroxine Sodium Tablets 150 Mcg (0.15 mg) Bottle Labels (Levothyroxine 125mcg)
Levothyroxine sodium is a prescription medication available in a quantity of 60 tablets with a strength of 125mcg/0.125mg per tablet. The manufacturer of the medication is Mylan and the lot number is 3049680. The medication was packaged by DOH Central Pharmacy located in Tallahassee, Florida. The expiration date of the medication is April 1st, 2014. There is an additional lot number mentioned as DO LOT # 10012013.G3. The text also contains a code, which is 303781813105.*
Levothyroxine Sodium Tablets 150 Mcg (0.15 mg) Bottle Labels (Levothyroxine 150mcg)
Levothyroxine sodium is a medication used to treat an underactive thyroid gland. It comes in tablet form and contains 150 micrograms (0.15 milligrams) of the active ingredient. The prescription is marked as "Rxon" and includes a code number. The remaining text is not legible and appears to be gibberish.*
Levothyroxine Sodium Tablets 75 Mcg (0.075 mg) Bottle Labels (Levothyroxine 75mcg)
LEVOTHYROXINE sodiBum is a prescription medication used to treat an underactive thyroid gland (hypothyroidism). The medication contains 0.075mg of the active ingredient and is only available with a prescription.*
* 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.
