Metoprolol Tartrate And Hydrochlorothiazide Tablet
Product Images NDC 62756-369

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Metoprolol Tartrate And Hydrochlorothiazide (NDC 62756-369). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Hctz-chem-str (Hctz Chem Str)

Hctz-chem-str (Hctz Chem Str)
Chemical structure diagram of Metoprolol Tartrate and Hydrochlorothiazide showing the molecular arrangement including a chlorinated aromatic ring, sulfonamide group, ketone group, and amine substitutions consistent with these active ingredients.*
FDA Label Image

Metoprolol-chem-str (Metoprolol Chem Str)

Metoprolol-chem-str (Metoprolol Chem Str)
Chemical structure of Metoprolol Tartrate and Hydrochlorothiazide depicted as a molecular diagram showing the arrangement of atoms and functional groups for the compound.*
FDA Label Image

Spl-metoprolol-tartrate-hydrochlorothiazide-label1 (Spl Metoprolol Tartrate Hydrochlorothiazide Label1)

Spl-metoprolol-tartrate-hydrochlorothiazide-label1 (Spl Metoprolol Tartrate Hydrochlorothiazide Label1)
Label for Metoprolol Tartrate and Hydrochlorothiazide Tablets, USP, showing strength 50 mg/25 mg. The label states that each tablet contains metoprolol tartrate USP 50 mg and hydrochlorothiazide USP 25 mg with storage instructions and usual dosage advice. The label indicates packaging of 100 tablets, Rx only, distributed by Sun Pharmaceutical Industries, Inc., Cranbury, NJ, and manufactured by Sun Pharmaceutical Industries Limited in India.*
FDA Label Image

Spl-metoprolol-tartrate-hydrochlorothiazide-label2 (Spl Metoprolol Tartrate Hydrochlorothiazide Label2)

Spl-metoprolol-tartrate-hydrochlorothiazide-label2 (Spl Metoprolol Tartrate Hydrochlorothiazide Label2)
Label for Metoprolol Tartrate and Hydrochlorothiazide Tablets, USP 100 mg/25 mg oral tablets. The label states packaging of 100 tablets, indicates Rx only, and lists Sun Pharmaceutical Industries, Inc. as the distributor and manufacturer. Storage instructions and dosage information references are also included.*
FDA Label Image

Spl-metoprolol-tartrate-hydrochlorothiazide-label3 (Spl Metoprolol Tartrate Hydrochlorothiazide Label3)

Spl-metoprolol-tartrate-hydrochlorothiazide-label3 (Spl Metoprolol Tartrate Hydrochlorothiazide Label3)
Label for Metoprolol Tartrate and Hydrochlorothiazide Tablets USP 100 mg/50 mg, oral tablet formulation. The label indicates a quantity of 100 tablets and is distributed by Sun Pharmaceutical Industries, Inc. Storage instructions and usual dosage advisory are visible, along with bar code and manufacturing details.*

* 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.