Magnesium Sulfate
- Product NDC
- 71872-7229
- 11-digit product format
- 718727229
- Labeler code
- 71872
- Product ID
- 71872-7229_b6352e51-468d-6d96-e053-2995a90ade1b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MAGNESIUM SULFATE HEPTAHYDRATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- NDA019316
- Marketing category
- NDA
- Marketing start
- 2000-08-08
- Substance
- MAGNESIUM SULFATE HEPTAHYDRATE
- Active strength
- 500 mg/mL
- Pharmacologic classes
- Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| SK47B8698T | MAGNESIUM SULFATE HEPTAHYDRATE | 10034-99-8 | MAGNESIUM SULFATE HEPTAHYDRATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7229-1 | 71872722901 | 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7229-1) / 10 mL in 1 VIAL, SINGLE-DOSE | 2020-10-13 | No | No | Historical |