Hydrochlorothiazide Capsule
Product Images NDC 70518-2550

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydrochlorothiazide (NDC 70518-2550). 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-01 (Hydrochlorothiazide Str)

Figure-01 (Hydrochlorothiazide Str)
Chemical structure diagram of Hydrochlorothiazide showing the molecular arrangement including sulfonamide groups, chlorine atom, and nitrogen-containing rings.*
FDA Label Image

Hydrochlorothiazide 12.5mg 70518 2550 00

Hydrochlorothiazide 12.5mg 70518 2550 00
Hydrochlorothiazide 12.5 mg capsules packaging label showing a quantity of 30 capsules. The label includes the NDC number 70518-2550-00 and states the product is repackaged by RemedyRepack Inc. It advises users to see the package insert for directions and includes storage temperature instructions.*
FDA Label Image

Hydrochlorothiazide 12.5mg 70518 2550 01

Hydrochlorothiazide 12.5mg 70518 2550 01
Hydrochlorothiazide 12.5 mg capsule label showing quantity of 90 capsules. Label includes NDC 70518-2550-01, manufacturer ScieGen Pharmaceuticals, and repackager RemedyRepack Inc. Directions reference package insert, with storage instructions from 20-25°C. Label displays a QR code and advises keeping medication out of reach of children.*
FDA Label Image

Hydrochlorothiazide 12.5mg 70518 2550 02

Hydrochlorothiazide 12.5mg 70518 2550 02
Label for Hydrochlorothiazide 12.5 mg oral capsules, quantity 60, repackaged by RemedyRepack Inc. The label includes manufacturer information for ScieGen Pharmaceuticals, Inc., a QR code, NDC 70518-2550-02, and basic storage directions. It states 'RX ONLY' and instructs to see 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.