Synthroid Tablet
Product Images NDC 0074-6624

20 FDA label images from Abbvie Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 20 technical images submitted to the FDA as part of the official labeling for Synthroid (NDC 0074-6624). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Abbvie 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

Synthroid Spl 01

Synthroid Spl 01
Chemical structure of Levothyroxine Sodium, the active ingredient in Synthroid tablets, showing the iodine-substituted phenol rings and amino acid side chain with sodium carboxylate group.*
FDA Label Image

Synthroid Spl 02

Synthroid Spl 02
Synthroid 50 mcg (0.05 mg) Levothyroxine Sodium oral tablets, USP, in a carton designed to hold 100 tablets. The packaging is labeled for AbbVie Inc. and includes a tamper-evident warning, storage instructions, and a notice that the package is for households without young children. The carton features barcodes and placeholders for lot, expiration, serial number, and 2D barcode information.*
FDA Label Image

Synthroid Spl 03

Synthroid Spl 03
Packaging label for Synthroid 100 mcg (0.1 mg) Levothyroxine Sodium tablets, USP. This box contains 100 oral tablets and is labeled for AbbVie Inc. It includes storage instructions, tamper-evident warnings, and a barcode, and specifies that the package is for households without young children.*
FDA Label Image

Synthroid Spl 04

Synthroid Spl 04
The packaging label for Synthroid 200 mcg (0.2 mg) tablets, USP, containing Levothyroxine Sodium. The label indicates a package size of 100 oral tablets. It includes storage instructions, a tamper-evident warning, and is labeled for household use without young children. The labeler is AbbVie Inc., North Chicago, IL, with NDC 0074-7148-11. Barcodes and placeholders for lot, expiration, and serial numbers are also present.*
FDA Label Image

Synthroid Spl 05

Synthroid Spl 05
Synthroid 137 mcg (0.137 mg) Levothyroxine Sodium Tablets, USP, oral dosage form, labeled in a package containing 90 tablets. The label includes dosage strength, directions for storage and handling, and manufacturer information for AbbVie Inc. The package also features a barcode and a placeholder area for lot and expiration information.*
FDA Label Image

Synthroid Spl 06

Synthroid Spl 06
Label for Synthroid 25 mcg (0.025 mg) Levothyroxine Sodium Tablets, USP, oral dosage form. The label indicates a package of 1000 tablets, labeled by AbbVie Inc. It includes instructions to not accept if the seal is broken and storage conditions at 25°C with permitted excursions. The label also features barcodes and regulatory information.*
FDA Label Image

Synthroid Spl 07

Synthroid Spl 07
Label for Synthroid Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg) oral tablets. The label shows that the package contains 1000 tablets and includes storage instructions, manufacturer AbbVie Inc., and cautions about container sealing and light protection. The NDC number 0074-5182-19 is displayed along with dosage and dispensing notes.*
FDA Label Image

Synthroid Spl 08

Synthroid Spl 08
Synthroid 88 mcg (0.088 mg) Levothyroxine Sodium Tablets, USP oral tablets. The label shows a package containing 90 tablets, labeled for prescription use only by AbbVie Inc. Storage instructions and dosing warnings are included on the label along with the NDC 0074-6594-90.*
FDA Label Image

Synthroid Spl 09

Synthroid Spl 09
Synthroid 125 mcg (0.125 mg) Levothyroxine Sodium Tablets, USP oral dosage form, packaged as 1000 tablets. Label includes storage instructions, dispensing warnings, and manufacturer information for AbbVie Inc.*
FDA Label Image

Synthroid Spl 0a

Synthroid Spl 0a
Synthroid 150 mcg (0.15 mg) Levothyroxine Sodium Tablets USP oral dosage form packaging label. The label indicates a bottle containing 90 tablets, manufactured by AbbVie Inc., with directions emphasizing storage at controlled room temperature and protection from light and moisture. The label also includes prescription-only status and a barcode.*
FDA Label Image

Synthroid Spl 0b

Synthroid Spl 0b
Synthroid 175 mcg (0.175 mg) Levothyroxine Sodium Tablets, USP, oral tablet form, in a package of 1000 tablets. The label includes storage instructions to keep at 25°C with permitted excursions and to protect from light and moisture. Manufactured by AbbVie Inc., North Chicago, IL, U.S.A., with NDC 0074-7070-19.*
FDA Label Image

Synthroid Spl 0c

Synthroid Spl 0c
Synthroid 300 mcg (0.3 mg) Levothyroxine Sodium Tablets USP, oral tablets, 90 count bottle packaging label. The label includes dosage strength, quantity, Rx only designation, AbbVie Inc. as the labeler, and storage instructions. A small blue round tablet image is shown on the label.*
FDA Label Image

Synthroid Spl 0d

Synthroid Spl 0d
Synthroid 112 mcg (0.112 mg) Levothyroxine Sodium Tablets USP in oral tablet form. The label shows a single round pink tablet and indicates a quantity of 1000 tablets. The product is labeled by AbbVie Inc. with storage instructions and handling precautions included.*
FDA Label Image

Synthroid Spl 0e

Synthroid Spl 0e
Synthroid 25 mcg (0.025 mg) levothyroxine sodium tablets, USP oral tablet packaging label. The label shows the AbbVie Inc. labeler and includes website information, dosage strength, color identifier (orange), and notation for household use without young children. The package is for 2 cards of 7 tablets each, marked as a professional sample not for sale, and prescription only.*
FDA Label Image

Synthroid Spl 0f

Synthroid Spl 0f
Synthroid 50 mcg (0.05 mg) Levothyroxine Sodium Tablets, USP label for oral tablets. The label indicates a bottle containing 90 tablets, distributed by AbbVie Inc. Instructions and storage information are printed on the label, along with a barcode and a placeholder for lot, expiration, serial number, and 2D barcode.*
FDA Label Image

Synthroid Spl 10

Synthroid Spl 10
Synthroid 75 mcg oral tablets packaging label showing AbbVie Inc. as labeler. The folded carton layout displays the proprietary name Synthroid, generic name Levothyroxine sodium tablets, USP, dosage strength of 75 mcg per tablet, and warnings such as "This package for households without young children." It also includes a barcode, QR code, and instructions for savings offers.*
FDA Label Image

Synthroid Spl 11

Synthroid Spl 11
Synthroid 112 mcg oral tablets carton label by AbbVie Inc. The label shows formulation as levothyroxine sodium tablets (USP) with a strength of 112 mcg per tablet. Packaging warnings specify it is a household package without young children. The label includes a barcode, QR code for patient safety information, and dosage instructions emphasize daily oral use. Branding and regulatory information are also displayed.*
FDA Label Image

Synthroid Spl 12

Synthroid Spl 12
Synthroid 200 mcg (0.2 mg) Levothyroxine Sodium Tablets USP label from AbbVie Inc. The label indicates a 90-tablet package and includes directions for proper storage and handling, emphasizing the tablet strength and prescription status.*
FDA Label Image

Synthroid Spl 13

Synthroid Spl 13
Synthroid 100 mcg oral tablets packaging label showing the brand and generic names (Levothyroxine Sodium), strength (100 mcg), tablet dosage form, and AbbVie Inc. as the labeler. The label features dosage information, a barcode, and a QR code, with additional details about savings programs and usage instructions.*
FDA Label Image

Synthroid Spl 14

Synthroid Spl 14
Label for Synthroid Levothyroxine Sodium Tablets USP, 100 mcg (0.1 mg) strength, containing 90 tablets. The label includes a barcode, a 2D barcode, and storage instructions to keep the product at controlled room temperature. The product is for oral use and is manufactured by AbbVie Inc.*

* 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.