Chlorothiazide Sodium Injection, Powder, Lyophilized, For Solution
Product Images NDC 47335-330

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Chlorothiazide Sodium (NDC 47335-330). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Chlorothiazide-sodium-structure (Chlorothiazide Na St)

FDA Label Image

Chlorothiazide-carton (Chlorothiazide Carton)

Chlorothiazide-carton (Chlorothiazide Carton)
This text describes Chlorothiazide Sodium, a sterile lyophilized powder used for the preparation of intravenous solutions. The active ingredient is 500mg of Chlorothiazide USP, and the usual adult dosage is 500mg once daily. It is to be reconstituted with a minimum of 18mL of sterile water for injection. This product comes in single-dose vials and should be used immediately after preparation. The reconstituted solution is clear and essentially free from visible particles. The text also includes important information about proper storage and disposal.*
FDA Label Image

Chlorothiazide-structure (Chlorothiazide Str)

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