Hydrochlorothiazide Tablet
Product Images NDC 63187-441

3 FDA label images from Proficient Rx Lp · 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 Hydrochlorothiazide (NDC 63187-441). 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.

Product Images & Figures Index

FDA Label Image

63187-441-30 (63187 441 30)

63187-441-30 (63187 441 30)
Label for Hydrochlorothiazide 50 mg oral tablets, packaged quantity of 30 tablets. The label shows the NDC 63187-441-30 and identifies the manufacturer as Excellium Pharmaceutical, Inc., Fairfield, NJ. The labeler is Proficient Rx LP, Thousand Oaks, CA. Tablets are described as round, peach, bisected, debossed EP 130. Storage instructions specify 20°-25°C (68°-77°F).*
FDA Label Image

Hydrochlorothiazide 25mg (Hydrochlorothiazide 25mg100tabs)

Hydrochlorothiazide 25mg (Hydrochlorothiazide 25mg100tabs)
Label for Hydrochlorothiazide 25 mg tablets by Proficient Rx LP. The label indicates a package of 30 peach, round, bisected tablets debossed with EP 131. Manufactured by Excellium Pharmaceutical, Inc. Storage instructions specify 20°-25°C (68°-77°F). Contains NDC 63187-440-30 and advises to keep medication out of the reach of children.*
FDA Label Image

Hydrochlorothiazide Structure (Hydrochlorothiazide Str)

Hydrochlorothiazide Structure (Hydrochlorothiazide Str)
Chemical structure of Hydrochlorothiazide, showing the arrangement of atoms including chlorine, sulfur, nitrogen, oxygen, and hydrogen. The formula C7H8ClN3O4S2 and molecular weight 297.74 are displayed below the structure.*

* 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.