Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 72189-012

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Losartan Potassium And Hydrochlorothiazide (NDC 72189-012). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct_rx, 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

040-90 (040 90)

Label for LOSARTAN POT/HCTZ 50/12.5 mg film-coated tablets, containing 50 mg losartan potassium and 12.5 mg hydrochlorothiazide. The package contains 90 tablets. Distributed by Direct_Rx, with lot number, expiration date, and manufacturing details visible. The label includes a barcode and storage instructions.*

FDA Label Image

98 (72189 098 90)

Packaging label for LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE film coated tablets, 100 mg/12.5 mg strength. The label shows a package containing 90 tablets, distributed by Direct Rx. It references the brand HYZAAR and indicates each film-coated tablet contains 100 mg losartan potassium and 12.5 mg hydrochlorothiazide. The label also includes lot number, expiration date (11/30/21), and relevant NDC numbers.*

FDA Label Image

129 (72189 129 90)

Losartan Potassium and Hydrochlorothiazide 50 mg / 12.5 mg film-coated tablets, 90 count. The label indicates it is generic for Hyzaar and states that each tablet contains 50 mg Losartan Potassium USP and 12.5 mg Hydrochlorothiazide USP. Packaged and distributed by Direct Rx, with manufacturing information by Jubilant Cadista Pharm Inc. The label includes lot number, expiration date, and storage instructions.*

FDA Label Image

139 (72189 139 30)

Packaging label for Losartan Potassium and Hydrochlorothiazide tablets, 100 mg/25 mg strength, film-coated, oral tablets. The label indicates a package size of 30 tablets and generic reference to Hyzaar. The labeler is Direct_Rx, with lot number 11SE2007 and expiration date 11/30/21. Manufacturer details and NDC information are also shown on the label.*

FDA Label Image

90 (72189 167 90)

Label for LOSARTAN POT./HCTZ 100/12.5 mg film-coated tablets, containing 90 tablets per package. The product is generic for HYZAAR and contains losartan potassium 100 mg and hydrochlorothiazide 12.5 mg. The label shows packaging and distribution by Direct Rx, along with lot number, production, and expiration details.*

FDA Label Image

30 (72189 167 30)

LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE 100/12.5 mg film-coated tablets by Direct_Rx. The carton contains 30 tablets. The front panel prominently shows the dosage strength and quantity with the proprietary name abbreviated as LOSARTAN POT./HCTZ. Manufacturer and batch details are included on the label.*

FDA Label Image

72189-129-30 (72189 129 30)

Losartan Potassium and Hydrochlorothiazide 50 mg / 12.5 mg film-coated tablets in a carton containing 30 tablets. The label shows the generic equivalent name Hyzaar with each tablet containing Losartan Potassium USP 50 mg and Hydrochlorothiazide USP 12.5 mg. The product is packaged and distributed by Direct Rx, with lot number and expiration date information included.*

FDA Label Image

72189-139-90 (72189 139 90)

Packaging label for Losartan Potassium and Hydrochlorothiazide 100 mg / 25 mg film-coated tablets. The label indicates a quantity of 90 tablets. It notes the product is generic for Hyzaar and lists the active ingredients with their strengths: Losartan Potassium USP 100 mg and Hydrochlorothiazide USP 25 mg. The label includes lot number, expiration date, manufacturer (Direct Rx), and NDC codes.*

* 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.