Methylergonovine Maleate Injection
Product Images NDC 51662-1556

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Methylergonovine Maleate (NDC 51662-1556). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Serialized Label (51662 1556 1 Serialized Labeling)

Serialized Label (51662 1556 1 Serialized Labeling)
METHYLERGONOVINE MALEATE 0.2 mg/mL injection in a single-dose amber glass ampule. The label shows the drug name, strength, and injection route, with distribution information by HF Acquisition Co LLC, DBA HealthFirst. The ampule includes a barcode and batch information on an attached label.*
FDA Label Image

Ampule Label (Ampule Labeling)

Ampule Label (Ampule Labeling)
Label for Methylergonovine Maleate Injection USP, 0.2 mg/mL, a prescription intravenous injection product. The label includes dosage strength, usage information for IM, OR, and IV routes, and storage instructions. It also shows distribution and manufacturing details by Breckenridge Pharmaceutical, Inc., Berlin, CT, and notes that the product is made in Poland. The label features a barcode and placeholders for lot number and expiration date.*
FDA Label Image

Description (Description)

Description (Description)
Chemical structure diagram of methylergonovine maleate, showing the molecular framework including aromatic rings, nitrogen atoms, and carboxylic acid groups characteristic of this active ingredient.*
FDA Label Image

Hs (How Supplied)

Hs (How Supplied)
A small table showing packaging information for a pharmaceutical product labeled as 1 mL size. It specifies the packaging configuration as boxes of 10 and includes an NDC code 51991-144-17. No product name or active ingredient is visible in the image.*

* 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.