magnesium sulfate
Generic: magnesium sulfate
Labeler: henry schein, inc.Drug Facts
Product Profile
Brand Name
magnesium sulfate
Generic Name
magnesium sulfate
Labeler
henry schein, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
magnesium sulfate heptahydrate 500 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0404-9902
Product ID
0404-9902_3eacd64d-fec5-4c18-a80a-d87231610738
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA019316
Listing Expiration
2026-12-31
Marketing Start
2022-01-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04049902
Hyphenated Format
0404-9902
Supplemental Identifiers
RxCUI
UNII
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 (source: ndc)
Application Number
NDA019316 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 BAG (0404-9902-20) / 20 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "3eacd64d-fec5-4c18-a80a-d87231610738", "openfda": {"unii": ["SK47B8698T"], "rxcui": ["1658236"], "spl_set_id": ["c255b8a9-68da-49c1-897b-bc18b731e459"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9902-20) / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9902-20", "marketing_start_date": "20220112"}], "brand_name": "Magnesium Sulfate", "product_id": "0404-9902_3eacd64d-fec5-4c18-a80a-d87231610738", "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": "0404-9902", "generic_name": "Magnesium Sulfate", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Magnesium Sulfate", "active_ingredients": [{"name": "MAGNESIUM SULFATE HEPTAHYDRATE", "strength": "500 mg/mL"}], "application_number": "NDA019316", "marketing_category": "NDA", "marketing_start_date": "20220112", "listing_expiration_date": "20261231"}