Phentermine Hydrochloride Capsule
Product Images NDC 42806-524

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Phentermine Hydrochloride (NDC 42806-524). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Epic 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.

Product Images & Figures Index

FDA Label Image

37 5 100

37 5 100
Label for PHENTERMINE HYDROCHLORIDE Capsules USP 37.5 mg by Epic Pharma, LLC. The label shows the NDC 42806-524-01, dosage strength of 37.5 mg, and package count of 100 capsules. It includes storage instructions, cautions about container integrity, and a warning to keep the medication out of reach of children. The label features Epic Pharma's logo and company address in Laurelton, NY.*
FDA Label Image

37 5 1000

37 5 1000
Label for Phentermine Hydrochloride Capsules, USP 37.5 mg by Epic Pharma, LLC. The label includes dosage form as capsules, highlights the strength of 37.5 mg, and specifies a package size of 1000 capsules. Instructions note storage at 20°-25°C, child-resistant packaging, and dispensing in a tight, light-resistant container. It also includes safety instructions such as keeping tightly closed and out of reach of children.*
FDA Label Image

Structural-formula (Structural Formula)

Structural-formula (Structural Formula)
Chemical structure diagram of phentermine hydrochloride showing its molecular arrangement including a benzene ring, methyl groups, and the amine (NH2) functional group bound to a hydrochloride (HCl) component.*

* 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.