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United States · US · US:66220-637_c78db5de-683f-41bd-8f25-700b9d0e2e46
SANCUSO
Orange BookUNIISPLATC A04AA02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCumberland Pharmaceuticals Inc.
CountryUS (United States)
ATC codeA04AA02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc116622063731168 h in 1 POUCH (66220-637-31)
- ndc116622063772168 h in 1 POUCH (66220-637-72)
Annotations
UNII (FDA Substance ID)
WZG3J2MCOL
GRANISETRON
RxCUI 26237
Orange Book
N022198
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "WZG3J2MCOL",
"rxcui": "26237",
"inchikey": "MFWNKCLOYSRHCJ-BTTYYORXSA-N",
"display_name": "GRANISETRON",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TRANSDERMAL",
"spl_meta": {
"7379369a-03df-4ec3-8f2e-66645cc736d8": {
"match": "brand_token",
"title": "SANCUSO (GRANISETRON) PATCH [CUMBERLAND PHARMACEUTICALS INC.]",
"spl_version": "4",
"published_date": "2024-11-05"
}
},
"productid": "66220-637_c78db5de-683f-41bd-8f25-700b9d0e2e46",
"productndc": "66220-637",
"dosage_form": "PATCH",
"orange_book": {
"appl_no": "022198",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "3.1MG/24HR",
"product_no": "001",
"approval_date": "Sep 12, 2008"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "GRANISETRON",
"proprietary_name": "SANCUSO",
"active_ingred_unit": "mg/24h",
"application_number": "NDA022198",
"marketing_category": "NDA",
"nonproprietary_name": "granisetron",
"start_marketing_date": "20240716",
"active_numerator_strength": "3.1"
}Related drugs
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