Hydrochlorothiazide Tablet
Product Images NDC 69315-155

9 FDA label images from Leading Pharma, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Hydrochlorothiazide (NDC 69315-155). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Leading Pharma, Llc, 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

12.5 mg 1000 Count Label (12point5mg1000ct)

12.5 mg 1000 Count Label (12point5mg1000ct)
Label of HYDROCHLOROTHIAZIDE 12.5 mg tablets, USP by Leading Pharma, LLC. The label states prescription use only with a package quantity of 1000 tablets. It includes dosage strength, manufacturer information, storage instructions, and a barcode.*
FDA Label Image

12.5 mg 100 Count Label (12point5mg100ct)

12.5 mg 100 Count Label (12point5mg100ct)
Label for HYDROCHLOROTHIAZIDE tablets USP 12.5 mg oral dosage form by Leading Pharma, LLC. The label indicates the product contains 100 tablets, is Rx only, and includes usage, storage, and manufacture information. The packaging features a barcode and the NDC 69315-155-01.*
FDA Label Image

25 mg 1000 Count Label (25mg1000ct)

25 mg 1000 Count Label (25mg1000ct)
Label for HYDROCHLOROTHIAZIDE tablets, USP, 25 mg strength, oral dosage form. The label indicates a package containing 1000 tablets, labeled for prescription use (Rx only). The manufacturer is Leading Pharma, LLC. The label includes standard storage and handling instructions along with a barcode and NDC number.*
FDA Label Image

25 mg 100 Count Label (25mg100ct)

25 mg 100 Count Label (25mg100ct)
Label for HYDROCHLOROTHIAZIDE tablets USP, 25 mg strength, with 100 tablets per bottle. Manufactured by Leading Pharma, LLC. The label includes dosage form as oral tablets, Rx only indication, and storage instructions at controlled room temperature. A barcode and NDC number 69315-131-01 are also visible.*
FDA Label Image

25 mg 5000 Count Label (25mg5000ct)

25 mg 5000 Count Label (25mg5000ct)
Label for HYDROCHLOROTHIAZIDE 25 mg tablets, USP, oral dosage form. The label shows a 5000 tablet package size and indicates the product is prescription only. It is manufactured by Leading Pharma, LLC, Fairfield, NJ 07004. The label includes storage instructions and a barcode.*
FDA Label Image

50 mg 1000 Count Label (50mg1000ct)

50 mg 1000 Count Label (50mg1000ct)
Label for HYDROCHLOROTHIAZIDE Tablets, USP 50 mg by Leading Pharma, LLC. The label indicates prescription use only with a quantity of 1000 tablets. It includes usage and storage instructions, manufacturer information, and a barcode.*
FDA Label Image

50 mg 100 Count Label (50mg100ct)

50 mg 100 Count Label (50mg100ct)
Label for HYDROCHLOROTHIAZIDE tablets, USP 50 mg oral tablets. The label indicates a prescription-only product with 100 tablets in the container, manufactured by Leading Pharma, LLC. It includes dosage and storage instructions, a barcode, and the NDC number 69315-130-01.*
FDA Label Image

Bulk

Bulk
This text panel provides packaging and storage information for Hydrochlorothiazide Tablets USP, 25 mg from Leading Pharma LLC. It includes net weight, average tablet weight, estimated tablet count per box, storage temperature guidelines, packaging deadlines, and verification fields for release and packaging dates.*
FDA Label Image

Chem Structure (Chemstructure)

Chem Structure (Chemstructure)
Chemical structure diagram of Hydrochlorothiazide showing its molecular formula C7H8ClN3O4S2 and molecular weight 297.74.*

* 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.