Magnesium Sulfate Injection, Solution
Product Images NDC 76483-129

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Magnesium Sulfate (NDC 76483-129). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Square Pharmaceuticals Plc., 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

Vial 1 G/2 mL (878a167e 0654 43a3 9d0b 3e5b4724e257 01)

Label for Magnesium Sulfate Injection, USP 50% solution with strength 1 gram per 2 mL (500 mg per mL) in a 2 mL single-dose vial from Square Pharmaceuticals PLC. Intended for intramuscular or intravenous use with dilution required before intravenous administration. The label includes storage instructions, sterile status, and manufacturing details.*

FDA Label Image

Carton 1 G/2 mL (878a167e 0654 43a3 9d0b 3e5b4724e257 02)

Magnesium Sulfate Injection, USP 50% (1 gram per 2 mL, 500 mg per mL) single-dose vials by Square Pharmaceuticals PLC. The label shows 25 vials of 2 mL each. The product contains magnesium sulfate heptahydrate 500 mg per 2 mL with additional information on storage, dilution requirement before intravenous use, and preservatives. The NDC is 76483-129.*

FDA Label Image

Vial 5 G/10 mL (878a167e 0654 43a3 9d0b 3e5b4724e257 03)

Magnesium Sulfate Injection, USP 50% (500 mg/mL) solution in a 10 mL single-dose vial. For intramuscular or intravenous use, label instructs the solution must be diluted before intravenous administration. Manufactured by Eskayef Pharmaceuticals Ltd. and labeled by Square Pharmaceuticals PLC., with storage instructions at 20° to 25°C.*

FDA Label Image

Carton 5 G/10 mL (878a167e 0654 43a3 9d0b 3e5b4724e257 04)

Packaging label for Magnesium Sulfate Injection, USP 500 mg/mL (5 grams per 10 mL) by Square Pharmaceuticals PLC. It is a sterile injection solution for intramuscular or intravenous use, sold in single-dose 10 mL vials with 25 vials per pack. The label includes dilution instructions and storage conditions at 20°C to 25°C.*

FDA Label Image

Vial 10 G/20 mL (878a167e 0654 43a3 9d0b 3e5b4724e257 05)

Magnesium Sulfate Injection, USP 500 mg/mL (10 grams per 20 mL) in a single-dose vial. The label indicates it is a 50% solution for intramuscular or intravenous use, sold by Square Pharmaceuticals PLC and Eskayef Pharmaceuticals Ltd. Storage instructions and sterilization details are printed along with a barcode and NDC 76483-129-04.*

FDA Label Image

Carton 10 G/20 mL (878a167e 0654 43a3 9d0b 3e5b4724e257 06)

Packaging label for Magnesium Sulfate Injection, USP 500 mg/mL (10 gram per 20 mL), an intramuscular and intravenous solution. The label indicates a 50% strength, requires dilution before intravenous use, and is preservative-free. It includes storage instructions and manufacturer details for Square Pharmaceuticals PLC, Bangladesh, with a package size of 2 single-dose 20 mL vials.*

FDA Label Image

Vial 25 G/50 mL (878a167e 0654 43a3 9d0b 3e5b4724e257 07)

Label for Magnesium Sulfate Injection, USP, 500 mg/mL (25 grams per 50 mL) injectable solution. The 50 mL single-dose vial is for intramuscular or intravenous use, with a warning to dilute before intravenous use. Labeler is Square Pharmaceuticals PLC, manufactured by Eskayef Pharmaceuticals Ltd, Bangladesh. The label includes storage instructions and sterility information.*

FDA Label Image

Carton 25 G/50 mL (878a167e 0654 43a3 9d0b 3e5b4724e257 08)

Label for Magnesium Sulfate Injection, USP 50% solution with 25 grams per 50 mL (500 mg/mL) strength. The injection solution is preservative-free and intended for intramuscular or intravenous use. The label includes dosage instructions, storage conditions, and manufacturer details from Square Pharmaceuticals PLC, Bangladesh. The package contains 2 vials of 50 mL each, single-dose vials, Rx only.*

* 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.