🇺🇸
United States · US · US:24338-177_50f23abd-6a66-44cb-960e-d43c16a5ae5f
SUPREP Bowel Prep
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
- ndc1124338177012 BOTTLE, PLASTIC in 1 CARTON (24338-177-01) / 133.1 mL in 1 BOTTLE, PLASTIC
Annotations
UNII (FDA Substance ID)
DE08037SAB
MAGNESIUM SULFATE, UNSPECIFIED FORM
RxCUI 6585
Orange Book
N022372
AA
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "DE08037SAB",
"rxcui": "6585",
"inchikey": null,
"display_name": "MAGNESIUM SULFATE, UNSPECIFIED FORM",
"substance_type": "mixture",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"50f23abd-6a66-44cb-960e-d43c16a5ae5f": {
"match": "brand_token",
"title": "SUPREP BOWEL PREP (SODIUM SULFATE, POTASSIUM SULFATE, MAGNESIUM SULFATE) SOLUTION, CONCENTRATE [AZURITY PHARMACEUTICALS, INC.]",
"spl_version": "1",
"published_date": "2026-04-02"
}
},
"productid": "24338-177_50f23abd-6a66-44cb-960e-d43c16a5ae5f",
"productndc": "24338-177",
"dosage_form": "SOLUTION, CONCENTRATE",
"orange_book": {
"appl_no": "022372",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AA",
"strength": "1.6GM/BOT;3.13GM/BOT;17.5GM/BOT",
"product_no": "001",
"approval_date": "Aug 5, 2010"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "MAGNESIUM SULFATE, UNSPECIFIED FORM; POTASSIUM SULFATE; SODIUM SULFATE",
"proprietary_name": "SUPREP Bowel Prep",
"active_ingred_unit": "g/133.1mL; g/133.1mL; g/133.1mL",
"application_number": "NDA022372",
"marketing_category": "NDA",
"nonproprietary_name": "sodium sulfate, potassium sulfate, magnesium sulfate",
"start_marketing_date": "20260401",
"active_numerator_strength": "1.2; 2.35; 13.13"
}Related drugs
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