magnesium sulfate

Generic: magnesium sulfate heptahydrate

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

Drug Facts

Product Profile

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

magnesium sulfate heptahydrate 4 g/100mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 0338-1715
Product ID 0338-1715_4607ad92-bf37-439d-92ec-51ee3cdf8318
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211966
Listing Expiration 2027-12-31
Marketing Start 2020-06-01

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 03381715
Hyphenated Format 0338-1715

Supplemental Identifiers

RxCUI
829734 1658259 1658262 2731632
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 (source: ndc)
Generic Name magnesium sulfate heptahydrate (source: ndc)
Application Number ANDA211966 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 4 g/100mL
source: ndc
Packaging
  • 40 BAG in 1 CARTON (0338-1715-40) / 100 mL in 1 BAG
source: ndc

Packages (1)

0338-1715-40 40 BAG in 1 CARTON (0338-1715-40) / 100 mL in 1 BAG

Ingredients (1)

magnesium sulfate heptahydrate (4 g/100mL)

Linked Drug Pages (1)

Magnesium Sulfate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "4607ad92-bf37-439d-92ec-51ee3cdf8318", "openfda": {"unii": ["SK47B8698T"], "rxcui": ["829734", "1658259", "1658262", "2731632"], "spl_set_id": ["ea05b8f9-6e11-45c3-824a-4a78818019df"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "40 BAG in 1 CARTON (0338-1715-40)  / 100 mL in 1 BAG", "package_ndc": "0338-1715-40", "marketing_start_date": "20200601"}], "brand_name": "Magnesium Sulfate", "product_id": "0338-1715_4607ad92-bf37-439d-92ec-51ee3cdf8318", "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": "0338-1715", "generic_name": "Magnesium Sulfate Heptahydrate", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Magnesium Sulfate", "active_ingredients": [{"name": "MAGNESIUM SULFATE HEPTAHYDRATE", "strength": "4 g/100mL"}], "application_number": "ANDA211966", "marketing_category": "ANDA", "marketing_start_date": "20200601", "listing_expiration_date": "20271231"}