magnesium sulfate

Generic: magnesium sulfate

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name magnesium sulfate
Generic Name magnesium sulfate
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

magnesium sulfate heptahydrate 500 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1372
Product ID 51662-1372_ef7bd6e6-d631-7e93-e053-2a95a90aef83
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019316
Listing Expiration 2026-12-31
Marketing Start 2019-10-14

Pharmacologic Class

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]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621372
Hyphenated Format 51662-1372

Supplemental Identifiers

RxCUI
1658236
UNII
SK47B8698T

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name magnesium sulfate (source: ndc)
Generic Name magnesium sulfate (source: ndc)
Application Number NDA019316 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/mL
source: ndc
Packaging
  • 20 mL in 1 VIAL, SINGLE-DOSE (51662-1372-1)
source: ndc

Packages (1)

51662-1372-1 20 mL in 1 VIAL, SINGLE-DOSE (51662-1372-1)

Ingredients (1)

magnesium sulfate heptahydrate (500 mg/mL)

Linked Drug Pages (1)

MAGNESIUM SULFATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "ef7bd6e6-d631-7e93-e053-2a95a90aef83", "openfda": {"unii": ["SK47B8698T"], "rxcui": ["1658236"], "spl_set_id": ["94e9a33f-39c4-4bc5-e053-2a95a90a43ac"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL, SINGLE-DOSE (51662-1372-1)", "package_ndc": "51662-1372-1", "marketing_start_date": "20191014"}], "brand_name": "MAGNESIUM SULFATE", "product_id": "51662-1372_ef7bd6e6-d631-7e93-e053-2a95a90aef83", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["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]"], "product_ndc": "51662-1372", "generic_name": "MAGNESIUM SULFATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MAGNESIUM SULFATE", "active_ingredients": [{"name": "MAGNESIUM SULFATE HEPTAHYDRATE", "strength": "500 mg/mL"}], "application_number": "NDA019316", "marketing_category": "NDA", "marketing_start_date": "20191014", "listing_expiration_date": "20261231"}