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United States · US · US:0338-1709_4361aea0-1a32-4c9a-86fb-d15f097eb0cc
MAGNESIUM SULFATE IN DEXTROSE
Orange BookUNIISPLATC D11AX05
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBaxter Healthcare Corporation
CountryUS (United States)
ATC codeD11AX05
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11033817094040 BAG in 1 CASE (0338-1709-40) / 100 mL in 1 BAG
Annotations
UNII (FDA Substance ID)
SK47B8698T
MAGNESIUM SULFATE HEPTAHYDRATE
RxCUI 236741
Orange Book
A211965
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "SK47B8698T",
"rxcui": "236741",
"inchikey": "WRUGWIBCXHJTDG-UHFFFAOYSA-L",
"display_name": "MAGNESIUM SULFATE HEPTAHYDRATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"9875ae6b-2d91-49a3-9512-60a2b8bbccda": {
"match": "brand_token",
"title": "MAGNESIUM OXIDE TABLET [BRYANT RANCH PREPACK]",
"spl_version": "103",
"published_date": "2026-05-25"
}
},
"productid": "0338-1709_4361aea0-1a32-4c9a-86fb-d15f097eb0cc",
"productndc": "0338-1709",
"dosage_form": "INJECTION, SOLUTION",
"orange_book": {
"appl_no": "211965",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "1GM/100ML",
"product_no": "001",
"approval_date": "Aug 11, 2020"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "MAGNESIUM SULFATE HEPTAHYDRATE",
"proprietary_name": "MAGNESIUM SULFATE IN DEXTROSE",
"active_ingred_unit": "mg/mL",
"application_number": "ANDA211965",
"marketing_category": "ANDA",
"nonproprietary_name": "magnesium sulfate in dextrose",
"start_marketing_date": "20200811",
"active_numerator_strength": "10"
}Related drugs
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