Lytensopril-90
Product Images NDC 68405-007

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lytensopril-90 (NDC 68405-007). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Physician Therapeutics 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

Hypertensa Label (Hypertensalabel)

Drug information panel for Hypertensa Medical Food by Physician Therapeutics LLC, detailing directions for use, storage instructions, warnings, and ingredients. The panel states it is for adults, taken as two capsules twice daily under physician supervision, and lists a proprietary amino acid blend plus additional ingredients. It also includes storage conditions and a warning to keep out of reach of children.*

FDA Label Image

Lisinoprillabel (Lisinoprillabel)

The image shows a label for Lisinopril 20 mg tablets manufactured by Lupin with lot number LSN01ZL and an expiration date of 11/08. The label includes a caution about federal law and handling instructions, a statement to take as directed by a doctor or see the outer packaging for dosage details, and references the medication Zestril for comparison. The label notes a 30-tablet quantity and includes barcodes and the manufacturer Hu Manix Co., Inc., Nipomo, CA.*

FDA Label Image

Lisinopril Structural Formula (Lisinoprilstructuralformula)

Chemical structure diagram of the active ingredient in Lytensopril-90, showing its molecular arrangement with associated atoms and bonds, including a depiction of 2 molecules of water of hydration.*

FDA Label Image

Lytensopril-90 (Lytensopril 90)

Label for Lytensopril-90 by Physician Therapeutics LLC, featuring a co-pack of Hypertensa 90 capsules and Lisinopril 20 mg, 30 tablets. The label states it requires physician authorization for refills and includes the NDC 68405-007-36. The design is split with light blue and white backgrounds and the Physician Therapeutics logo.*

* 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.