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United States · US · US:24338-201_c020e973-dccf-4862-999e-17db6209a48a
SUTAB
Orange BookUNIISPLATC C03CB
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAzurity Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeC03CB
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1124338201012 BOTTLE, PLASTIC in 1 KIT (24338-201-01) / 12 TABLET in 1 BOTTLE, PLASTIC
Annotations
UNII (FDA Substance ID)
ML30MJ2U7I
MAGNESIUM SULFATE ANHYDROUS
RxCUI 1311625
Orange Book
N213135
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "ML30MJ2U7I",
"rxcui": "1311625",
"inchikey": "CSNNHWWHGAXBCP-UHFFFAOYSA-L",
"display_name": "MAGNESIUM SULFATE ANHYDROUS",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"c020e973-dccf-4862-999e-17db6209a48a": {
"match": "brand_token",
"title": "SUTAB (SODIUM SULFATE, MAGNESIUM SULFATE, AND POTASSIUM CHLORIDE) TABLET [AZURITY PHARMACEUTICALS, INC.]",
"spl_version": "1",
"published_date": "2026-04-02"
}
},
"productid": "24338-201_c020e973-dccf-4862-999e-17db6209a48a",
"productndc": "24338-201",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "213135",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "0.225GM;0.188GM;1.479GM",
"product_no": "001",
"approval_date": "Nov 10, 2020"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "MAGNESIUM SULFATE ANHYDROUS; POTASSIUM CHLORIDE; SODIUM SULFATE",
"proprietary_name": "SUTAB",
"active_ingred_unit": "g/1; g/1; g/1",
"application_number": "NDA213135",
"marketing_category": "NDA",
"nonproprietary_name": "sodium sulfate, magnesium sulfate, and potassium chloride",
"start_marketing_date": "20260401",
"active_numerator_strength": "2.7; 2.25; 17.75"
}Related drugs
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