Phentermine Hydrochloride Capsule
Product Images NDC 11534-159

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Phentermine Hydrochloride (NDC 11534-159). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sunrise Pharmaceutical, 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

59600473-figure-01 (59600473 Figure 01)

A data table displaying Body Mass Index (BMI) values in kg/m² based on weight in pounds (from 140 to 250) and height in feet and inches (from 5'0" to 6'3"). The table cells contain corresponding BMI numbers for various combinations of height and weight.*

FDA Label Image

59600473-figure-02 (59600473 Figure 02)

Chemical structure of phentermine hydrochloride, showing its molecular arrangement including a phenyl ring attached to a carbon with methyl and amine groups, connected to hydrochloride.*

FDA Label Image

59600473-figure-03 (59600473 Figure 03)

Phentermine hydrochloride 37.5 mg oral tablets by Sunrise Pharmaceutical, Inc. The white tablet contains 37.5 mg phentermine hydrochloride with 30 tablets per container. Label includes storage instructions, warnings about abuse and safety precautions, and NDC 11534-160-30.*

FDA Label Image

59600473-figure-04 (59600473 Figure 04)

Label of Phentermine Hydrochloride Capsules USP 37.5 mg by Sunrise Pharmaceutical, Inc. The label indicates 100 capsules per bottle, with each capsule containing 30 mg phentermine base equivalent to 37.5 mg phentermine hydrochloride. The label includes usage and safety warnings about prescription use, child-resistant packaging, and storage instructions.*

* 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.