magnesium chloride

Generic: magnesium chloride

Labeler: mylan institutional llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name magnesium chloride
Generic Name magnesium chloride
Labeler mylan institutional llc
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

magnesium chloride 200 mg/mL

Manufacturer
Mylan Institutional LLC

Identifiers & Regulatory

Product NDC 67457-134
Product ID 67457-134_46f389a6-b16b-44af-b468-973805cc3c49
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2013-03-14

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 67457134
Hyphenated Format 67457-134

Supplemental Identifiers

RxCUI
311422
UNII
02F3473H9O

Packaging Origin

Original Packager
true

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 chloride (source: ndc)
Generic Name magnesium chloride (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 200 mg/mL
source: ndc
Packaging
  • 1 VIAL, MULTI-DOSE in 1 CARTON (67457-134-50) / 50 mL in 1 VIAL, MULTI-DOSE
source: ndc

Packages (1)

67457-134-50 1 VIAL, MULTI-DOSE in 1 CARTON (67457-134-50) / 50 mL in 1 VIAL, MULTI-DOSE

Ingredients (1)

magnesium chloride (200 mg/mL)

Linked Drug Pages (1)

Magnesium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "46f389a6-b16b-44af-b468-973805cc3c49", "openfda": {"unii": ["02F3473H9O"], "rxcui": ["311422"], "spl_set_id": ["2105d1c1-54ef-4d1a-a63c-b1619e8b50db"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (67457-134-50)  / 50 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "67457-134-50", "marketing_start_date": "20130314"}], "brand_name": "Magnesium Chloride", "product_id": "67457-134_46f389a6-b16b-44af-b468-973805cc3c49", "dosage_form": "INJECTION", "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": "67457-134", "generic_name": "magnesium chloride", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Magnesium Chloride", "active_ingredients": [{"name": "MAGNESIUM CHLORIDE", "strength": "200 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20130314", "listing_expiration_date": "20261231"}