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United States · US · US:63304-479_558c3230-3788-4ef0-a5b5-3c06870317a9
Cevimeline
Orange BookUNIISPLATC N07AX03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSun Pharmaceutical Industries, Inc.
CountryUS (United States)
ATC codeN07AX03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc116330447901100 CAPSULE in 1 BOTTLE (63304-479-01)
Annotations
UNII (FDA Substance ID)
P81Q6V85NP
CEVIMELINE HYDROCHLORIDE
RxCUI 260036
Orange Book
N020989
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "P81Q6V85NP",
"rxcui": "260036",
"inchikey": "ZSTLCHCDLIUXJE-ZGBAEQJLSA-N;ZSTLCHCDLIUXJE-GMLJRNIPSA-N",
"display_name": "CEVIMELINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"bcaaec18-4ee1-4cfd-84da-8fe3b8c54fc4": {
"match": "brand_token",
"title": "CEVIMELINE HYDROCHLORIDE CAPSULE [ASCLEMED USA INC.]",
"spl_version": "1",
"published_date": "2026-05-21"
}
},
"productid": "63304-479_558c3230-3788-4ef0-a5b5-3c06870317a9",
"productndc": "63304-479",
"dosage_form": "CAPSULE",
"orange_book": {
"appl_no": "020989",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "30MG",
"product_no": "002",
"approval_date": "Jan 11, 2000"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CEVIMELINE HYDROCHLORIDE",
"proprietary_name": "Cevimeline",
"active_ingred_unit": "mg/1",
"application_number": "NDA020989",
"marketing_category": "NDA",
"nonproprietary_name": "Cevimeline",
"start_marketing_date": "20160310",
"active_numerator_strength": "30"
}Related drugs
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