Ephedrine Sulfate Injection
Product Images NDC 70756-611

3 FDA label images from Lifestar Pharma Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ephedrine Sulfate (NDC 70756-611). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lifestar Pharma Llc, 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 (Abbedc8b C9b5 4049 A31b Dbffb73c6556 01)

Structural Formula (Abbedc8b C9b5 4049 A31b Dbffb73c6556 01)
Chemical structure diagram of ephedrine sulfate, showing two ephedrine molecules paired with one sulfuric acid (H2SO4) molecule as the sulfate component.*
FDA Label Image

1 mL Vial Label (Abbedc8b C9b5 4049 A31b Dbffb73c6556 02)

1 mL Vial Label (Abbedc8b C9b5 4049 A31b Dbffb73c6556 02)
Label for Ephedrine Sulfate Injection, USP 50 mg/mL, an intravenous single-dose vial. The label states that the product must be diluted before use and is prescription only. It is manufactured for Lifestar Pharma LLC, located in Mahwah, NJ, and marked as made in India. The label includes dosage details, lot, and expiration date fields as well as a barcode.*
FDA Label Image

25-count Carton Label (Abbedc8b C9b5 4049 A31b Dbffb73c6556 03)

25-count Carton Label (Abbedc8b C9b5 4049 A31b Dbffb73c6556 03)
Packaging label for Ephedrine Sulfate Injection, USP 50 mg/mL, an intravenous injection product by Lifestar Pharma LLC. The label indicates the need for dilution before use, single-dose vial packaging (25 x 1 mL vials), discard unused portion instructions, and storage conditions. The label includes the NDC 70756-611-25 and manufacturing information.*

* 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.