Magnesium Sulfate

Product NDC

70518-0950

11-digit product format

705180950

Labeler code

70518

Product ID

70518-0950_6286e9f4-fd74-7a02-e053-2991aa0a3ef6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

MAGNESIUM SULFATE HEPTAHYDRATE

Dosage form

INJECTION, SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

REMEDYREPACK INC.

Application

NDA019316

Marketing category

NDA

Marketing start

2018-01-11

Marketing end

0000-00-00

Substance

MAGNESIUM SULFATE HEPTAHYDRATE

Active strength

500 mg/mL

Pharmacologic classes

Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record