Neostigmine Methylsulfate Injection
Product Images NDC 0548-9602

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Neostigmine Methylsulfate (NDC 0548-9602). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amphastar Pharmaceuticals, 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

Carton 10 mg/10 mL (Carton 10mg)

Carton 10 mg/10 mL (Carton 10mg)
Box label for Neostigmine Methylsulfate Injection, USP 1 mg/mL (10 mg/10 mL) by Amphastar Pharmaceuticals, Inc. The vial is for intravenous use, 10 mL multiple dose. The label includes storage instructions, formulation details, and directions to see the package insert. NDC code 0548-9602-00 is printed.*
FDA Label Image

Carton 5 mg/10 mL (Carton 5mg)

Carton 5 mg/10 mL (Carton 5mg)
Label for NEOSTIGMINE METHYLSULFATE Injection, USP 5 mg/10 mL (0.5 mg/mL) intravenous injection from Amphastar Pharmaceuticals, Inc. The label includes dosage strength, directions to see package insert, storage instructions to protect from light and keep between 20° to 25°C, with allowances for excursions, and lists phenol as preservative and sodium acetate trihydrate in the formulation. It is indicated for use in a 10 mL multiple dose vial with NDC 0548-9601-00.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of neostigmine methylsulfate, featuring a quaternary ammonium group, aromatic ring, ester linkage, and methyl groups, consistent with the active ingredient in NEOSTIGMINE METHYLSULFATE injection.*

* 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.