Valproate Sodium Injection
Product Images NDC 0143-9785

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Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Valproate Sodium (NDC 0143-9785). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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 (Valproate Sodium Injection 1)

Chemical Structure (Valproate Sodium Injection 1)
Chemical structure diagram of valproate sodium, showing its carbon, hydrogen, oxygen atoms, and sodium ion. The structure depicts the molecule's arrangement with a carboxylate group linked to a branched hydrocarbon chain.*
FDA Label Image

Figure 1 (Valproate Sodium Injection 2)

Figure 1 (Valproate Sodium Injection 2)
A line graph comparing the percentage reduction in CPS rate against the percentage of patients for Divalproex Sodium versus placebo. The vertical axis represents improvement (positive reduction) or worsening (negative reduction) in CPS rate, with no change at zero. The horizontal axis shows the percentage of patients from 0 to 100.*
FDA Label Image

Figure 2 (Valproate Sodium Injection 3)

Figure 2 (Valproate Sodium Injection 3)
A chart showing the percentage reduction in CPS rate versus the percentage of patients for Valproate Sodium at high and low doses. The vertical axis represents percent reduction in CPS rate with directions for improvement and worsening, and the horizontal axis shows the percentage of patients from 0 to 100%. Two curves compare high dose (solid line) and low dose (dotted line) effects.*
FDA Label Image

Ndc 0143-9785-01 Valproate Sodium Injection, Usp 500 mg/5 mL (100 mg/ml) For Iv Infusion Only Rx Only 5 mL Single Dose Vial Each mL Contains: Valproic Acid 100 mg, Edetate Disodium 0.4 mg, And Water For Injection. Ph Adjusted With Sodium Hydroxide And/or Hydrochloric Acid. Usual Dosage: See Package Insert. Contains No Preservatives Discard Any Unused Solution. Store At 20º To 25ºc (68º To 77ºf) [see Usp Controlled Room Temperature]. (Valproate Sodium Injection 4)

Ndc 0143-9785-01 Valproate Sodium Injection, Usp 500 mg/5 mL (100 mg/ml) For Iv Infusion Only Rx Only 5 mL Single Dose Vial Each mL Contains: Valproic Acid 100 mg, Edetate Disodium 0.4 mg, And Water For Injection. Ph Adjusted With Sodium Hydroxide And/or Hydrochloric Acid. Usual Dosage: See Package Insert. Contains No Preservatives Discard Any Unused Solution. Store At 20º To 25ºc (68º To 77ºf) [see Usp Controlled Room Temperature]. (Valproate Sodium Injection 4)
Label for Valproate Sodium Injection, USP 500 mg per 5 mL (100 mg/mL) in a 5 mL single-dose vial. It is preservative-free and intended for intravenous infusion only. The label includes active ingredient details, storage instructions, manufacturer Hikma Farmacêutica (Portugal), and distributor Hikma Pharmaceuticals USA Inc.*
FDA Label Image

Plb782-wes/2 (Valproate Sodium Injection 5)

Plb782-wes/2 (Valproate Sodium Injection 5)
Valproate Sodium Injection, USP 500 mg per 5 mL (100 mg/mL) label for intravenous use. The label shows it is preservative-free, for infusion only, supplied in 10 single-dose 5 mL vials. Manufactured by Hikma Farmacêutica (Portugal), distributed by Hikma Pharmaceuticals USA Inc. Includes dosing, storage, and handling instructions, and a barcode.*
FDA Label Image

Valproate Sodium Injection 6

Valproate Sodium Injection 6
Label panel for Valproate Sodium Injection 500 mg/5mL by Hikma Pharmaceuticals USA Inc. The label includes a QR code, GTIN number 00301234567896, serial number 1234567890123, a placeholder expiration date, and lot number ABCDE12345.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.