Quetiapine Tablet
Product Images NDC 43547-522

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Quetiapine (NDC 43547-522). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Solco Healthcare Us, 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.

FDA Label Image

17db564c-figure-01 (Image 01)

Label for Quetiapine Tablets, USP 25 mg oral tablets by Solco Healthcare US, LLC. The label indicates it is a prescription-only medication with 100 tablets per container. It includes storage instructions and manufacturer details from Zhejiang Huahai Pharmaceutical Co., Ltd., China.*

FDA Label Image

17db564c-figure-02 (Image 02)

Quetiapine Tablets, USP 50 mg oral tablets label by Solco Healthcare US, LLC. The label indicates each film-coated tablet contains 50 mg quetiapine (equivalent to 57.56 mg quetiapine fumarate). The packaging includes NDC 43547-519-10, directions for storage, warnings, manufacturing by Zhejiang Huahai Pharmaceutical Co., and a 100-tablet count.*

FDA Label Image

17db564c-figure-03 (Image 03)

Quetiapine Tablets USP 100 mg label from Solco Healthcare US, LLC. The label includes a blue and yellow design with the product name and strength prominently displayed. It states the quantity as 100 tablets and includes storage instructions, manufacturer Zhejiang Huahai Pharmaceutical Co., Ltd., distributor Solco Healthcare US, LLC, and a barcode. The label also mentions prescription use and a medication guide website.*

FDA Label Image

25 mg (Image 04)

Quetiapine Tablets USP 200 mg oral film-coated tablets in a 100-tablet package. The label displays the drug name, strength, and prescribing warnings. Manufactured by Zhejiang Huahai Pharmaceutical Co., Ltd. and distributed by Solco Healthcare US, LLC.*

FDA Label Image

50 mg (Image 05)

Label for Quetiapine Tablets, USP 300 mg oral tablets, supplied in a 100-tablet package. The label states prescription use only (Rx only) and includes storage instructions, manufacturer Zhejiang Huahai Pharmaceutical Co., Ltd. in China, and distributor Solco Healthcare US, LLC. The label also provides a web address for the medication guide and barcode information.*

FDA Label Image

100 mg (Image 06)

Quetiapine Tablets, USP 400 mg film-coated oral tablets in a package containing 100 tablets. The label specifies storage conditions and includes manufacturer Zhejiang Huahai Pharmaceutical Co., Ltd, and distributor Solco Healthcare US, LLC. It also displays an NDC number, barcode, and a statement to dispense the medication guide to patients.*

FDA Label Image

200 mg (Image 07)

Packaging label for Quetiapine Tablets, USP, 200 mg oral tablets. The label shows a blue and white design with green highlights, indicating a bottle containing 100 tablets. The label includes dosage strength, manufacturer Zhejiang Huahai Pharmaceutical Co., Ltd. in China, and distributor Solco Healthcare US, LLC. It also has storage and warning information and a QR code for the medication guide.*

FDA Label Image

300 mg (Image 08)

Label for Quetiapine Tablets USP 300 mg oral tablets, packaged in a bottle of 60 tablets. The label shows the product name, strength, dosage form, and manufacturer details including Zhejiang Huahai Pharmaceutical Co., Ltd. It also includes storage instructions and a note to dispense the medication guide provided by Solco Healthcare US, LLC.*

FDA Label Image

400 mg (Image 09)

Label for Quetiapine Tablets, USP 400 mg, oral tablets by Solco Healthcare US, LLC. The label states the package contains 100 film-coated tablets. It includes storage instructions, a warning to keep out of reach of children, and manufacture details from Zhejiang Huahai Pharmaceutical Co., Ltd. The NDC is 43547-523-10.*

* 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.