Magnesium Sulfate
- Product NDC
- 71872-7055
- 11-digit product format
- 718727055
- Labeler code
- 71872
- Product ID
- 71872-7055_9ce57b9f-96b0-91b1-e053-2995a90a100c
- 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
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71872-7055-1 | 71872705501 | 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7055-1) > 2 mL in 1 VIAL, SINGLE-DOSE | 2018-02-28 | 0000-00-00 | No | No | Current |