Magnesium Sulfate

Generic: MAGNESIUM SULFATE HEPTAHYDRATE

Labeler: Mylan Institutional LLC
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive

Drug Facts

Product Profile

Brand Name Magnesium Sulfate
Generic Name MAGNESIUM SULFATE HEPTAHYDRATE
Labeler Mylan Institutional LLC
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

MAGNESIUM SULFATE HEPTAHYDRATE 2 g/50mL

Identifiers & Regulatory

Product NDC 67457-553
Product ID 67457-553_86b5c926-cd75-44bb-9cca-ea76e6916708
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209911
Marketing Start 2020-10-02
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67457553
Hyphenated Format 67457-553

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 HEPTAHYDRATE (source: ndc)
Application Number ANDA209911 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2 g/50mL
source: ndc
Packaging
  • 1 BAG in 1 POUCH (67457-553-00) / 50 mL in 1 BAG
source: ndc

Packages (1)

67457-553-00 1 BAG in 1 POUCH (67457-553-00) / 50 mL in 1 BAG

Ingredients (1)

MAGNESIUM SULFATE HEPTAHYDRATE (2 g/50mL)

Linked Drug Pages (1)

Magnesium Sulfate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "86b5c926-cd75-44bb-9cca-ea76e6916708", "openfda": {"unii": ["SK47B8698T"], "rxcui": ["1658259", "1658262"], "spl_set_id": ["297cae36-9935-4f7c-8039-5401992f5768"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BAG in 1 POUCH (67457-553-00)  / 50 mL in 1 BAG", "package_ndc": "67457-553-00", "marketing_end_date": "20260228", "marketing_start_date": "20201002"}], "brand_name": "Magnesium Sulfate", "product_id": "67457-553_86b5c926-cd75-44bb-9cca-ea76e6916708", "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": "67457-553", "generic_name": "MAGNESIUM SULFATE HEPTAHYDRATE", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Magnesium Sulfate", "active_ingredients": [{"name": "MAGNESIUM SULFATE HEPTAHYDRATE", "strength": "2 g/50mL"}], "application_number": "ANDA209911", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20201002"}