Cetrorelix Acetate Kit
Product Images NDC 67184-0605

Product Visual Gallery

This gallery contains 16 technical images submitted to the FDA as part of the official labeling for Cetrorelix Acetate (NDC 67184-0605). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Qilu Pharmaceutical Co., Ltd., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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Chemical Structure (Cetrorelix 01)

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Figure (Cetrorelix 02)

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Figure (Cetrorelix 03)

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Figure (Cetrorelix 04)

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Figure (Cetrorelix 05)

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Figure (Cetrorelix 06)

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Figure (Cetrorelix 07)

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Figure (Cetrorelix 08)

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Figure (Cetrorelix 09)

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Figure (Cetrorelix 10)

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Figure (Cetrorelix 11)

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Figure (Cetrorelix 12)

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Principal Display Panel (Carton)

This text provides detailed information about Cetrorelix Acetate for Injection, including dosage, administration instructions, storage conditions, and manufacturer details. It outlines the contents of one carton, such as vial, syringe with diluent, and needles, along with dosage information and precautions. It also includes contact information for medical advice and reporting side effects. Additionally, it mentions the composition of the vial and diluent.*

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Principal Display Panel (Tray kit)

This is a description of Cetrorelix Acetate for Injection. Each pack includes one vial of lyophilized powder for reconstitution, one pre-filled syringe with diluent, a 20-gauge needle, and a 27-gauge needle. The medication is for subcutaneous use only and should be stored refrigerated at 2°C to 8°C. Manufactured by QILU Pharmaceutical Co., Ltd. in Jinan, China. LOT number X00000XX, with an expiration date of MMYYYY. Reconstitute before use.*

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Principal Display Panel (Vial)

This text provides information about a medication called Cetrorelix Acetate. It includes the National Drug Code (NDC) 67184-0567-1 and advises to store the vial protected from light and refrigerated between 2°C to 8°C (36°F to 46°F). The medication is for subcutaneous use only and is manufactured by QILU Pharmaceutical Co., Ltd. in China. The vial contains 0.25 mg of the medication and is a single-dose format. The lot number and expiry date are required for prescription use.*

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Principal Display Panel (Diluent Syringe)

This is a prefilled sterile water for injection manufactured by QILU Pharmaceutical Co., Ltd. The product is intended for prescription use only and comes in a 1mL size. The label includes NDC code 67184-0568-1, manufacturing details, and information such as lot number and expiration date.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.