Magnesium Sulfate
- Product NDC
- 52584-754
- 11-digit product format
- 525840754
- Labeler code
- 52584
- Product ID
- 52584-754_32b9244c-5dce-4eb0-a80d-d644d161bf84
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Magnesium Sulfate Heptahydrate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- General Injectables & Vaccines, Inc
- Application
- ANDA075151
- Marketing category
- ANDA
- Marketing start
- 2010-08-01
- Marketing end
- 2024-02-01
- 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
- 0000-00-00
- 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 |
|---|
| 52584-754-10 | 52584075410 | 1 SYRINGE, PLASTIC in 1 BAG (52584-754-10) > 10 mL in 1 SYRINGE, PLASTIC | 2010-08-01 | 2024-02-01 | No | No | Current |