Lisinopril And Hydrochlorothiazide Tablet
Product Images NDC 70518-0196

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Lisinopril And Hydrochlorothiazide (NDC 70518-0196). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Figure 1 (3a53f18e Af9b 4932 8300 B3521e87528d 01)

Chemical structure diagram of Lisinopril dihydrate, the active ingredient in Lisinopril and Hydrochlorothiazide combination tablets, showing its molecular structure with atoms and bonds illustrated.*

FDA Label Image

Figure 2 (3a53f18e Af9b 4932 8300 B3521e87528d 02)

Chemical structure diagram depicting the molecular structure of hydrochlorothiazide, one of the active ingredients in Lisinopril and Hydrochlorothiazide tablets by Remedyrepack Inc.*

FDA Label Image

Mm2 (Lisinopril Hctz 10mg 12.5mg 70518 0196 01)

Label for Lisinopril and Hydrochlorothiazide 10 mg / 12.5 mg tablets, quantity 90. The label includes a barcode, QR code, and states RX ONLY, with NDC 70518-0196-01. Manufactured by Lupin Pharma, Baltimore, MD, and repackaged by RemedyRepack Inc. Storage instructions and a caution to keep medication out of reach of children are also visible.*

FDA Label Image

Mm3 (Lisinopril Hctz 10mg 12.5mg 70518 0196 02)

Label for Lisinopril and Hydrochlorothiazide 10 mg / 12.5 mg oral tablets, quantity 90. The label includes the product name, strength, dosage form, quantity, NDC number 70518-0196-02, and manufacturer information showing Lupin Pharma, Baltimore, MD, with repackaging by RemedyRepack Inc. storage instructions are also provided.*

FDA Label Image

Remedy_label (Remedy Label)

Label for Lisinopril and Hydrochlorothiazide 10 mg/12.5 mg oral tablets. The package contains 30 tablets. The label includes the NDC number 70518-0196-00 and states the product is RX only. Manufactured by Lupin Pharma, repackaged by RemedyRepack Inc. It advises storage at 20-25°C and refers users to the package insert for directions.*

* 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.