Levoxyl Tablet
Product Images NDC 60793-859

14 FDA label images from Pfizer Laboratories Div Pfizer Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 14 technical images submitted to the FDA as part of the official labeling for Levoxyl (NDC 60793-859). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pfizer Laboratories Div Pfizer 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

Chemical Structure (Levoxyl 01)

Chemical Structure (Levoxyl 01)
Chemical structure of levothyroxine sodium showing two iodinated aromatic rings connected by an ether linkage, with a side chain containing an amine group and a sodium carboxylate hydrate moiety.*
FDA Label Image

Logo (Levoxyl 01a)

FDA Label Image

Levoxyl 01b

FDA Label Image

Principal Display Panel (25 mcg Tablet Bottle Label)

Principal Display Panel (25 mcg Tablet Bottle Label)
Label for Levoxyl 25 mcg oral tablets by Pfizer Laboratories Div Pfizer Inc. The label indicates levothyroxine sodium tablets, USP, in a package containing 100 tablets. Storage instructions specify keeping the product between 68°F-77°F, with permitted excursions between 59°F-86°F. The label also notes dispensing in a tight, light-resistant, child-resistant container and states it is made in Austria.*
FDA Label Image

Principal Display Panel (50 mcg Tablet Bottle Label)

Principal Display Panel (50 mcg Tablet Bottle Label)
Levoxyl 50 mcg oral tablets label from Pfizer Laboratories Division Pfizer Inc. The label shows that it contains 100 tablets of levothyroxine sodium, USP. It includes dosage storage instructions, NDC number 60793-851-01, a barcode, and states the product is prescription only. The label also indicates the tablets are made in Austria.*
FDA Label Image

Principal Display Panel (75 mcg Tablet Bottle Label)

Principal Display Panel (75 mcg Tablet Bottle Label)
Levoxyl 75 mcg oral tablets label displaying the Pfizer logo. The label indicates levothyroxine sodium tablets, USP, with a package count of 100 tablets. Storage instructions and distributor information (Pfizer Inc, New York, NY) are included. The label also features barcodes, a National Drug Code (NDC 60793-852-01), and claims no imprint or varnish.*
FDA Label Image

Principal Display Panel (88 mcg Tablet Bottle Label)

Principal Display Panel (88 mcg Tablet Bottle Label)
Label for LEVOXYL 88 mcg levothyroxine sodium tablets, USP, distributed by Pfizer Laboratories Div Pfizer Inc. The label indicates a package containing 100 tablets for oral use, with storage instructions between 68°F-77°F. The label includes the Pfizer logo, NDC 60793-853-01, and regulatory markings.*
FDA Label Image

Principal Display Panel (100 mcg Tablet Bottle Label)

Principal Display Panel (100 mcg Tablet Bottle Label)
Levoxyl 100 mcg oral tablets package label by Pfizer Laboratories. The label indicates levothyroxine sodium USP tablets with a quantity of 100 tablets. It includes storage instructions and directs to refer to the package insert for dosage information. The label also shows the NDC and manufacturer details, noting the product is made in Austria.*
FDA Label Image

Principal Display Panel (112 mcg Tablet Bottle Label)

Principal Display Panel (112 mcg Tablet Bottle Label)
Levoxyl 112 mcg oral tablets label by Pfizer Laboratories, containing 100 tablets. The label states levothyroxine sodium tablets, USP, with dosage information including storage conditions and distribution details. Includes barcodes and a Pfizer logo.*
FDA Label Image

Principal Display Panel (125 mcg Tablet Bottle Label)

Principal Display Panel (125 mcg Tablet Bottle Label)
Label for LEVOXYL 125 mcg oral tablets containing levothyroxine sodium, distributed by Pfizer Inc. The label indicates the package contains 100 tablets and features storage instructions alongside NDC 60793-856-01 and barcodes. It is marked Rx only and notes the product is made in Austria.*
FDA Label Image

Principal Display Panel (137 mcg Tablet Bottle Label)

Principal Display Panel (137 mcg Tablet Bottle Label)
Levoxyl 137 mcg levothyroxine sodium tablets packaging label displaying the Pfizer logo. The label indicates this package contains 100 tablets for oral use and is prescription only. Storage instructions specify temperature ranges and container requirements. The product is distributed by Pfizer Inc., New York, and made in Austria.*
FDA Label Image

Principal Display Panel (150 mcg Tablet Bottle Label)

Principal Display Panel (150 mcg Tablet Bottle Label)
The image shows a Pfizer Levoxyl label for levothyroxine sodium tablets, USP, 150 mcg strength. The label indicates 100 tablets in the package and includes storage instructions, a UPC barcode, NDC number 60793-858-01, and distribution information noting Pfizer Inc., New York, NY. The label emphasizes prescription-only use and features imprint area details.*
FDA Label Image

Principal Display Panel (175 mcg Tablet Bottle Label)

Principal Display Panel (175 mcg Tablet Bottle Label)
Levoxl 175 mcg levothyroxine sodium tablets label from Pfizer Laboratories. The label indicates a bottle containing 100 tablets of oral dosage form. It includes dosage storage instructions, distribution details, barcode, NDC 60793-859-01, and a note on dispensing in child-resistant containers.*
FDA Label Image

Principal Display Panel (200 mcg Tablet Bottle Label)

Principal Display Panel (200 mcg Tablet Bottle Label)
Levoxl 200 mcg levothyroxine sodium tablets, USP, oral tablets in a package of 100 tablets. The label includes Pfizer Laboratories as the labeler, with packaging instructions noting storage temperature ranges and child-resistant container requirements. The label also shows the NDC number 60793-860-01 and states 'Rx only.'*

* 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.