magnesium sulfate in water
Generic: magnesium sulfate in water
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
magnesium sulfate in water
Generic Name
magnesium sulfate in water
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
magnesium sulfate heptahydrate 20 g/500mL
Manufacturer
Identifiers & Regulatory
Product NDC
0409-2050
Product ID
0409-2050_be314bfd-462e-4573-b902-d70fa062c55b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA020309
Listing Expiration
2027-12-31
Marketing Start
2022-11-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04092050
Hyphenated Format
0409-2050
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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 water (source: ndc)
Generic Name
magnesium sulfate in water (source: ndc)
Application Number
NDA020309 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 g/500mL
Packaging
- 20 POUCH in 1 CASE (0409-2050-20) / 1 BAG in 1 POUCH / 500 mL in 1 BAG (0409-2050-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "be314bfd-462e-4573-b902-d70fa062c55b", "openfda": {"unii": ["SK47B8698T"], "rxcui": ["829734", "1658259", "1658262", "1658264", "1658265"], "spl_set_id": ["22ca78b4-f5a3-4144-cf89-5f633acf1e6d"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 POUCH in 1 CASE (0409-2050-20) / 1 BAG in 1 POUCH / 500 mL in 1 BAG (0409-2050-01)", "package_ndc": "0409-2050-20", "marketing_start_date": "20221114"}], "brand_name": "Magnesium Sulfate in Water", "product_id": "0409-2050_be314bfd-462e-4573-b902-d70fa062c55b", "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": "0409-2050", "generic_name": "MAGNESIUM SULFATE IN WATER", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Magnesium Sulfate in Water", "active_ingredients": [{"name": "MAGNESIUM SULFATE HEPTAHYDRATE", "strength": "20 g/500mL"}], "application_number": "NDA020309", "marketing_category": "NDA", "marketing_start_date": "20221114", "listing_expiration_date": "20271231"}