Phentermine And Topiramate Extended-release Capsule
Product Images NDC 43598-627

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Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Phentermine And Topiramate Extended-release (NDC 43598-627). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr.reddys Laboratories 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

Container1 (Container1)

Container1 (Container1)
Phentermine and Topiramate Extended-Release Capsules 3.75 mg/23 mg label for a 30-capsule package by Dr. Reddy's Laboratories Inc. The label includes the NDC number 43598-624-30, instructions for the pharmacist to dispense the Medication Guide, storage conditions, and a barcode. It notes the product is Rx only and made in India.*
FDA Label Image

Container2 (Container2)

Container2 (Container2)
Label for Phentermine and Topiramate Extended-Release Capsules 7.5 mg/46 mg by Dr.Reddy's Laboratories Inc. The label indicates 30 capsules per container with NDC 43598-625-30. It includes dosage form as capsules, an Rx only designation, bar code, and storage instructions. The label also highlights pharmacist dispensing instructions for the Medication Guide.*
FDA Label Image

Container3 (Container3)

Container3 (Container3)
Label for Phentermine and Topiramate Extended-Release Capsules 11.25 mg/69 mg by Dr. Reddy's Laboratories Inc. The label states prescription use only and contains 30 capsules. It includes dosing information, storage instructions, a barcode, and the NDC 43598-626-30. The label also features pharmacist dispensing instructions and manufacturing details.*
FDA Label Image

Container4 (Container4)

Container4 (Container4)
Label for Phentermine and Topiramate Extended-Release Capsules 15 mg/92 mg by Dr. Reddy's Laboratories Inc. The label states the product is Rx only and contains 30 capsules. It includes dosage and storage information, a NDC number 43598-627-30, a barcode, and a pharmacist note to dispense the medication guide to patients.*
FDA Label Image

Figure (Figure)

Figure (Figure)
Illustrations showing four variations of Phentermine and Topiramate Extended-Release capsules, each with different color caps and imprint codes. Figure A shows a white capsule with black printing labeled DRL 624 (3.75 mg/23 mg). Figure B shows a capsule with a red cap and white body with black printing labeled DRL 625 (7.5 mg/46 mg). Figure C displays a capsule with a green cap and white body with black printing labeled DRL 626 (11.25 mg/69 mg). Figure D depicts a capsule with an orange cap and white body with black printing labeled DRL 627 (15 mg/92 mg).*
FDA Label Image

Figure1_figure2 (Figure1 Figure2)

Figure1_figure2 (Figure1 Figure2)
Two line graphs labeled Study 1 and Study 2 showing percent weight loss (LS Mean) over 56 weeks. Each graph compares placebo, phentermine and topiramate extended-release capsules 7.5 mg/46 mg, and 15 mg/92 mg groups. The x-axis represents time in weeks, and the y-axis shows percent weight loss, with greater losses in higher dose groups. Study completers and ITT-LOCF data points are displayed.*
FDA Label Image

Phenterminestructure (Phenterminestructure)

Phenterminestructure (Phenterminestructure)
Chemical structure diagram showing the molecular arrangement of the active ingredient Phentermine in the drug Phentermine and Topiramate Extended-Release.*
FDA Label Image

Topiramatestructure (Topiramatestructure)

Topiramatestructure (Topiramatestructure)
Chemical structure of topiramate, one of the active ingredients in Phentermine and Topiramate Extended-Release capsules, showing its molecular framework with sulfur, oxygen, carbon, and nitrogen atoms.*

* 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.