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Active Strength & Injectable PresentationCeftriaxone 250 mg Injection is generally presented as a sterile powder containing ceftriaxone sodium equivalent to 250 mg of ceftriaxone in a single-dose vial. The powder requires reconstitution with an approved diluent before administration by a qualified healthcare professional. Hospital and institutional buyers should verify the pharmacopoeial standard, route of administration, batch certificate of analysis (COA), sterility documentation and destination-market authorization before procurement.Composition & Physicochemical PropertiesThe vial contains ceftriaxone in the form of ceftriaxone sodium, typically supplied as a white to yellowish crystalline powder for solution for injection. Technical evaluation should cover identification, potency, related substances, water content, particulate matter, sterility, bacterial endotoxins and container-closure integrity against the approved specification. Compatible diluents, reconstitution instructions, solution stability and administration conditions must be confirmed from the manufacturer’s approved product information.

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Min. Order: 1 Unit

r k d pharmaceutical llp

GST

Mumbai, India

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