magnesium sulfate
- Product NDC
- 50090-3323
- 11-digit product format
- 500903323
- Labeler code
- 50090
- Product ID
- 50090-3323_fbb684de-0ce7-4d47-8c5c-6b464e7dccac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MAGNESIUM SULFATE HEPTAHYDRATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- A-S Medication Solutions
- Application
- ANDA206485
- Marketing category
- ANDA
- Marketing start
- 2016-03-15
- Marketing end
- 0000-00-00
- Substance
- MAGNESIUM SULFATE HEPTAHYDRATE
- Active strength
- 40 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