Micardis Hct
Product Images NDC 54868-5418

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Micardis Hct (NDC 54868-5418). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Physicians Total Care, 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

Micardis Hct 80 mg/12.5 mg 30 Tablets (4540)

Micardis Hct 80 mg/12.5 mg 30 Tablets (4540)
This is a prescription drug called "Hicardis HCT" distributed by Physicians Total Care. It comes in a package with National Drug Code (NDC) 54868-4540-2 and has a strength of 86/12.5mg. The lot number of this particular package is 6660 with an expiration date of BME 61/60. The text "weom e" and the number "45400930080" may not be related to the drug and its packaging information.*
FDA Label Image

Micardis Hct 80 mg/25 mg 30 Tablets (5297)

Micardis Hct 80 mg/25 mg 30 Tablets (5297)
This appears to be a label for the medication NICARDIS HCT 86/25HG, distributed by PHYSICIANS TOTAL CARE. The NDC (National Drug Code) for this medication is 54868-5297-8. The label also includes a LOT #0000 XD with a DATE of 61/60. It is unclear what the "T" and "52970300000" signify.*
FDA Label Image

Micardis Hct 40 mg/12.5 mg 30 Tablets (5418)

Micardis Hct 40 mg/12.5 mg 30 Tablets (5418)
The medication Hicardis HCT with a strength of 46/12.5mg and the lot number #0800 with an expiration date of 01/0 is distributed by Physicians Total Care and has the NDC code 54868-5418-0. The remaining text is not readable.*
FDA Label Image

Telmisartan Structure (Micardis Hct Struc01)

FDA Label Image

Telmisartan Structure (Micardis Hct Struc02)

* 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.