Triamterene And Hydrochlorothiazide Capsule
Product Images NDC 82804-308

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Triamterene And Hydrochlorothiazide (NDC 82804-308). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Image (Ba702c00 5dc6 4545 Bde9 Ff7dbb7fd1a7 01)

Image (Ba702c00 5dc6 4545 Bde9 Ff7dbb7fd1a7 01)
Chemical structure diagram showing a sulfonamide compound with chlorine (Cl), aminosulfonyl (NH2SO2), and other groups attached to a benzene ring, representing a component related to the active ingredients of Triamterene and Hydrochlorothiazide capsules.*
FDA Label Image

Image (Ba702c00 5dc6 4545 Bde9 Ff7dbb7fd1a7 02)

Image (Ba702c00 5dc6 4545 Bde9 Ff7dbb7fd1a7 02)
Chemical structure of the active ingredient Triamterene, showing its molecular framework including amino groups and aromatic rings.*
FDA Label Image

82804-308-30 (Image 01)

82804-308-30 (Image 01)
Label for Triamterene HCTZ 37.5 mg / 25 mg capsules, containing 30 capsules per bottle. The label includes detailed capsule description, showing the capsule is a size '4' gelatin with yellow opaque cap imprinted with '855' in black ink and a white opaque body. Manufactured by Zydus Lifesciences Ltd., India, and packaged by Proficient Rx LP, Thousand Oaks, CA. Storage temperature is 20°-25°C (68°-77°F). The label also features multiple barcodes and QR codes along with NDC 82804-308-30 and indicates prescription 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.