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
INTRAVENOUS
Active Ingredients

magnesium sulfate heptahydrate 40 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1352
Product ID 51662-1352_100d196c-c851-3cf7-e063-6294a90ad8c2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020309
Listing Expiration 2026-12-31
Marketing Start 2018-12-21

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 516621352
Hyphenated Format 51662-1352

Supplemental Identifiers

RxCUI
1658259
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 NDA020309 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 40 mg/mL
source: ndc
Packaging
  • 50 mL in 1 BAG (51662-1352-1)
  • 24 POUCH in 1 CASE (51662-1352-3) / 1 BAG in 1 POUCH (51662-1352-2) / 50 mL in 1 BAG
source: ndc

Packages (2)

51662-1352-1 50 mL in 1 BAG (51662-1352-1) 51662-1352-3 24 POUCH in 1 CASE (51662-1352-3) / 1 BAG in 1 POUCH (51662-1352-2) / 50 mL in 1 BAG

Ingredients (1)

magnesium sulfate heptahydrate (40 mg/mL)

Linked Drug Pages (1)

MAGNESIUM SULFATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "100d196c-c851-3cf7-e063-6294a90ad8c2", "openfda": {"unii": ["SK47B8698T"], "rxcui": ["1658259"], "spl_set_id": ["7d94995b-9e2a-0345-e053-2991aa0a62d0"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BAG (51662-1352-1)", "package_ndc": "51662-1352-1", "marketing_start_date": "20181221"}, {"sample": false, "description": "24 POUCH in 1 CASE (51662-1352-3)  / 1 BAG in 1 POUCH (51662-1352-2)  / 50 mL in 1 BAG", "package_ndc": "51662-1352-3", "marketing_start_date": "20220801"}], "brand_name": "MAGNESIUM SULFATE", "product_id": "51662-1352_100d196c-c851-3cf7-e063-6294a90ad8c2", "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": "51662-1352", "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": "40 mg/mL"}], "application_number": "NDA020309", "marketing_category": "NDA", "marketing_start_date": "20181221", "listing_expiration_date": "20261231"}