magnesium sulfate in dextrose

Generic: magnesium sulfate in dextrose

Labeler: baxter healthcare corporation
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name magnesium sulfate in dextrose
Generic Name magnesium sulfate in dextrose
Labeler baxter healthcare corporation
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

magnesium sulfate heptahydrate 10 mg/mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 0338-1709
Product ID 0338-1709_4361aea0-1a32-4c9a-86fb-d15f097eb0cc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211965
Listing Expiration 2026-12-31
Marketing Start 2020-08-11

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 03381709
Hyphenated Format 0338-1709

Supplemental Identifiers

RxCUI
829757
UNII
SK47B8698T

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 sulfate in dextrose (source: ndc)
Generic Name magnesium sulfate in dextrose (source: ndc)
Application Number ANDA211965 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 40 BAG in 1 CASE (0338-1709-40) / 100 mL in 1 BAG
source: ndc

Packages (1)

Ingredients (1)

magnesium sulfate heptahydrate (10 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "4361aea0-1a32-4c9a-86fb-d15f097eb0cc", "openfda": {"unii": ["SK47B8698T"], "rxcui": ["829757"], "spl_set_id": ["1bbaebd0-3f4c-467d-96fd-69cfad5a3fd3"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "40 BAG in 1 CASE (0338-1709-40)  / 100 mL in 1 BAG", "package_ndc": "0338-1709-40", "marketing_start_date": "20200811"}], "brand_name": "MAGNESIUM SULFATE IN DEXTROSE", "product_id": "0338-1709_4361aea0-1a32-4c9a-86fb-d15f097eb0cc", "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": "0338-1709", "generic_name": "magnesium sulfate in dextrose", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MAGNESIUM SULFATE IN DEXTROSE", "active_ingredients": [{"name": "MAGNESIUM SULFATE HEPTAHYDRATE", "strength": "10 mg/mL"}], "application_number": "ANDA211965", "marketing_category": "ANDA", "marketing_start_date": "20200811", "listing_expiration_date": "20261231"}