Phentolamine Mesylate Injection, Powder, For Solution
Product Images NDC 0143-9564

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Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Phentolamine Mesylate (NDC 0143-9564). 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

Structural Formula (Phentolamine Mesylate For Injection Usp 1)

Structural Formula (Phentolamine Mesylate For Injection Usp 1)
Chemical structure of phentolamine mesylate, showing the arrangement of its molecular components including aromatic rings and functional groups consistent with the active ingredient phentolamine mesylate.*
FDA Label Image

Ndc 0143-9564-01 Rx Only Phentolamine Mesylate For Injection, Usp 5 mg/vial For Im Or Iv Use Lyophilized Usual Dosage: See Package Insert Store At 20º To 25ºc (68º To 77ºf) [ See Usp Controlled Room Temperature]. (Phentolamine Mesylate For Injection Usp 2)

Ndc 0143-9564-01 Rx Only Phentolamine Mesylate For Injection, Usp 5 mg/vial For Im Or Iv Use Lyophilized Usual Dosage: See Package Insert Store At 20º To 25ºc (68º To 77ºf) [ See Usp Controlled Room Temperature]. (Phentolamine Mesylate For Injection Usp 2)
Phentolamine Mesylate 5 mg/mL injection powder for solution label. The label states it is for injection USP, for IM or IV use, and lyophilized. It indicates the product is manufactured by Hikma Pharmaceuticals USA Inc. and includes regulatory and barcode information.*
FDA Label Image

Ndc 0143-9564-10 Rx Only 10 X 2 mL Phentolamine Mesylate For Injection, Usp 5 mg/vial For Im Or Iv Use Lyophilized Each Vial Contains Phentolamine Mesylate Usp 5 mg And 25 mg Mannitol In Lyophilized Form. Usual Dosage: See Package Insert Store At 20º To 25ºc (68º To 77ºf) [ See Usp Controlled Room Temperature]. The Reconstituted Solution Should Be Used Upon Preparation And Should Not Be Stored. (Phentolamine Mesylate For Injection Usp 3)

Ndc 0143-9564-10 Rx Only 10 X 2 mL Phentolamine Mesylate For Injection, Usp 5 mg/vial For Im Or Iv Use Lyophilized Each Vial Contains Phentolamine Mesylate Usp 5 mg And 25 mg Mannitol In Lyophilized Form. Usual Dosage: See Package Insert Store At 20º To 25ºc (68º To 77ºf) [ See Usp Controlled Room Temperature]. The Reconstituted Solution Should Be Used Upon Preparation And Should Not Be Stored. (Phentolamine Mesylate For Injection Usp 3)
Packaging label for Phentolamine Mesylate 5 mg/vial injection, powder for solution, for intramuscular or intravenous use. The label includes storage instructions and notes that the solution should be used upon preparation. Manufactured by Hikma Farmaceutica (Portugal) and distributed by West-Ward. The vial size is 1 x 2 mL.*
FDA Label Image

Phentolamine Mesylate For Injection Usp 4

Phentolamine Mesylate For Injection Usp 4
Phentolamine Mesylate 5 mg/vial injection, powder for solution for intramuscular or intravenous use. The label indicates lyophilized formulation contained in 10 vials of 2 mL each. Manufactured by Hikma Farmaceutica (Portugal) and distributed by West-Ward, with storage instructions at controlled room temperature. The label includes dosage preparation and storage information along with barcodes and NDC 0143-9564-10.*
FDA Label Image

Phentolamine Mesylate For Injection Usp 5

Phentolamine Mesylate For Injection Usp 5
A label showing product identification details including a GTIN barcode with the number 00301234567896, a serial number 1234567890123, an expiration date placeholder marked as MMYYYY, and a lot number ABCDE12345. This label appears to be part of the packaging for Phentolamine Mesylate injection powder for solution.*

* 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.