Cetrorelix Acetate Kit
Product Images NDC 60505-6270

Product Visual Gallery

This gallery contains 16 technical images submitted to the FDA as part of the official labeling for Cetrorelix Acetate (NDC 60505-6270). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Apotex Corp., 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 is information about Cetrorelix Acetate for Injection, a medication used for subcutaneous use. The product includes one vial containing a specified amount of the active ingredient and mannitol, along with a pre-filled syringe and two different gauge needles. The medication should be stored refrigerated between 2°C to 8°C. It is manufactured by QILU Pharmaceutical Co., Ltd. in China and distributed by Apotex Corp. in Weston, FL.*

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Principal Display Panel (Tray kit)

This text describes a medication with National Drug Code (NDC) 60505-6270-1, containing Cetrorelix Acetate for Injection at 0.25 mg/vial for subcutaneous use. It includes a vial with lyophilized powder, a pre-filled syringe with diluent, a 20-gauge needle, and a 27-gauge needle. The medication should be stored in the refrigerator at 2°C to 8°C (36°F to 46°F). The manufacturer is QILU Pharmaceutical Co., Ltd. in Jinan, China, and the distributor is Apotex Corp. in Weston, FL. The lot number, revision date, and expiration date are also provided.*

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Principal Display Panel (Vial)

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Principal Display Panel (Diluent Syringe)

This is a description of a 1 mL prefilled sterile water for injection product. It is manufactured by Apotex Corp. and distributed by QILU Pharmaceutical Co., Ltd in China. The product is indicated by NDC 60505-6276-0 with code number 340401278048. The lot number and expiration date are labeled as "XXXXXXXXXX" and "YYYY/MM" respectively.*

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