NDC Compounded Drug 70004-731-30 Magnesium Sulfate Heptahydrate
Injection, Solution Intravenous
Compounded Drug Product Information
Frequently Asked Questions
What is the NDC number assigned to Magnesium Sulfate (2gm) Pf In 0.9% Sodium Chloride?
Magnesium Sulfate (2gm) Pf In 0.9% Sodium Chloride was assigned by its manufacturer with NDC product code 70004-731. This product is a drug classified as a human compounded drug. Compounded drugs are medications created by combining or altering existing drugs to meet the specific needs of certain patients. The NDC directory only includes information about compounded drugs from facilities that choose to assign NDC numbers to their products.
Which are the NDC package codes for Magnesium Sulfate (2gm) Pf In 0.9% Sodium Chloride?
The NDC package code 70004-731-30 was assigned to a 1 INJECTION, SOLUTION in 1 BAG of magnesium sulfate heptahydrate administered intravenous via injection, solution.
Who manufactures this product?
Magnesium Sulfate (2gm) Pf In 0.9% Sodium Chloride is manufactured by an outsourced facility and labeled by Sca Pharmaceuticals, Llc. All compounded drugs included in the NDC directory are classified as "Outsourcing Facility Compounded Human Drug Product (Exempt from Approval Requirements)". Outsourcing facilities are a type of drug compounding facility regulated under Section 503B of the FD&C Act could be eligible for exemptions from drug registration if they meet all the conditions specified under Section 503B.