Tygacil Injection, Powder, Lyophilized, For Solution
Product Images NDC 0008-4990

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Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tygacil (NDC 0008-4990). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer 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

Chemical Structure (Tygacil 01)

FDA Label Image

Logo (Tygacil 01a)

Logo (Tygacil 01a)
G2 miectables are a pharmaceutical product distributed by Wyeth Pharmaceuticals, a subsidiary of Pfizer Inc, based in Philadelphia, PA 19101.*
FDA Label Image

Principal Display Panel (50 mg Vial Label)

Principal Display Panel (50 mg Vial Label)
This text appears to be a medication label for Tygacil (Tigecycline) injection solutions. It includes the National Drug Code (NDC) 0008-4990-19, which indicates that the solution should be prescribed by a healthcare provider. The solution comes in a single-dose vial that is yellow to orange in color, and any unused solution should be discarded. The package insert should be consulted for complete instructions on use. The solution contains 100 mg of lactose monohydrate and is adjusted with HCl and possibly NaOH. This medication is distributed by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. The label includes a lot number (8920288RB) for identification purposes.*
FDA Label Image

Principal Display Panel (50 mg Vial Carton)

Principal Display Panel (50 mg Vial Carton)
This is a pharmaceutical product description for a medication called Tygacil, manufactured by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. The medication is lyophilized powder that requires reconstitution before administration, and is used for intravenous infusion. The product is available in 50mg single-dose vials, and the recommended dosage is an initial dose of 100mg, followed by 50mg every 12 hours. The reconstituted solution should be further diluted for IV infusion, and the resultant solution should contain 10 mg/mL. The reconstituted solution should be yellow to orange in color; If not, the solution should be discarded. The product contains lactose monohydrate and the pH is adjusted with hydrochloric acid and, if necessary, sodium pyridoxine, but it does not contain any preservatives. Storage temperature ranges from 20°C to 25°C.*

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