Phentermine Hydrochloride Tablet
Product Images NDC 10702-025

9 FDA label images from Kvk-tech, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Phentermine Hydrochloride (NDC 10702-025). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kvk-tech, 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

Bmi Index (Figure 1 Bmi Index)

Bmi Index (Figure 1 Bmi Index)
A data table presenting Body Mass Index (BMI) values in kg/m² by weight (pounds) and height (feet, inches). The table includes BMI calculations for weights from 140 to 250 pounds and heights from 5'0" to 6'3". Some BMI values are highlighted with boxes.*
FDA Label Image

Chemical Structure (Figure 2 Chemical Structure)

Chemical Structure (Figure 2 Chemical Structure)
Chemical structure of Phentermine Hydrochloride showing the molecular formula C10H15N·HCl and molecular weight 185.7. The diagram depicts the active ingredient's molecular arrangement, including a benzene ring and amine group.*
FDA Label Image
FDA Label Image

Caps 30s (Figure 4 Caps 30s)

Caps 30s (Figure 4 Caps 30s)
Phentermine Hydrochloride Capsules, USP 37.5 mg oral capsules label from KVK-TECH, Inc. The label specifies 30 capsules per container, includes dosage information, storage instructions, tamper-evident warning, and a barcode. The label also notes the product is prescription only and manufactured in the USA by KVK-Tech, Inc.*
FDA Label Image

37.5 mg Capsules 100s (Figure 5 Caps 100s)

37.5 mg Capsules 100s (Figure 5 Caps 100s)
Label for Phentermine Hydrochloride Capsules, USP 37.5 mg by KVK-TECH, Inc. The label shows the proprietary and generic name, strength, route of administration as oral capsules, and package size of 100 capsules. Instructions include storage conditions, child-resistant closure, and tamper-evident foil seal under the cap. The label displays the NDC 10702-029-01 and notes the product is for Rx only.*
FDA Label Image

37.5 mg Capsules 1000s (Figure 6 Caps 1000s)

37.5 mg Capsules 1000s (Figure 6 Caps 1000s)
Phentermine Hydrochloride Capsules USP 37.5 mg label for oral capsules. The label specifies 1000 capsules and includes storage instructions, tamper-evident details, dosage advisory to see package insert, and manufacturer information as KVK-Tech, Inc., Newtown, PA. The NDC is 10702-029-10.*
FDA Label Image

37.5 mg Tablets 30s (Figure 7 Tabs 30s)

37.5 mg Tablets 30s (Figure 7 Tabs 30s)
Phentermine Hydrochloride Tablets, USP 37.5 mg capsule label from KVK-TECH, Inc. The label provides dosage strength of 37.5 mg, packaging quantity of 30 tablets, and storage instructions. It includes tamper-evident foil seal information and barcode with NDC 10702-025-03. The label is for oral prescription use only.*
FDA Label Image

37.5 mg Tablets 100s (Figure 8 Tabs 100s)

37.5 mg Tablets 100s (Figure 8 Tabs 100s)
Phentermine Hydrochloride 37.5 mg capsules packaging label by KVK-TECH, Inc. The label indicates 100 tablets per container with NDC 10702-025-01. Usage instructions include storage between 20° to 25°C with permissible excursions and a child-resistant closure. Tamper evidence is provided by a foil seal under the cap.*
FDA Label Image

37.5 mg Tablets 1000s (Figure 9 Tabs 1000s)

37.5 mg Tablets 1000s (Figure 9 Tabs 1000s)
Label for Phentermine Hydrochloride Tablets, USP 37.5 mg by KVK-TECH, Inc. The label indicates each blue and white tablet contains 37.5 mg phentermine hydrochloride. It includes storage instructions (20° to 25°C), tamper-evident information, and packaging details for 1000 tablets. The label shows the NDC 10702-025-10 and the manufacturer location in Newtown, PA, USA.*

* 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.