Home NDC 67457-134 Magnesium Chloride
Product NDC 67457-134
11-digit product format 674570134
Labeler code 67457
Product ID 67457-134_46f389a6-b16b-44af-b468-973805cc3c49
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name magnesium chloride
Dosage form INJECTION
Route INTRAVENOUS
Labeler Mylan Institutional LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2013-03-14
Substance MAGNESIUM CHLORIDE
Active strength 200 mg/mL
Pharmacologic 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]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Magnesium Chloride
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MAGNESIUM CHLORIDE 200 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 02F3473H9O Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 311422 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 67457-134-50 Magnesium Chloride 50 mL in 1 VIAL, MULTI-DOSE INJECTION 50 7 67457-134-50 Magnesium Chloride 1 in 1 CARTON INJECTION 1 7
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67457-134 MAGNESIUM CHLORIDE INJECTION [MYLAN INSTITUTIONAL LLC] 7 Current NDC, Legacy NDC, 2 package rows 20211028_2105d1c1-54ef-4d1a-a63c-b1619e8b50db.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 67457-134-50 67457013450 1 VIAL, MULTI-DOSE in 1 CARTON (67457-134-50) / 50 mL in 1 VIAL, MULTI-DOSE 2013-03-14 0000-00-00 No No Current