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United States · US · US:0143-9392_5c5e498b-d829-4f78-bcca-466631014767
REMIFENTANIL HYDROCHLORIDE
In shortageOrange BookUNIISPLATC N01AH06
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHikma Pharmaceuticals USA Inc.
CountryUS (United States)
ATC codeN01AH06
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11014393921010 VIAL in 1 CARTON (0143-9392-10) / 5 mL in 1 VIAL (0143-9392-01)
Annotations
UNII (FDA Substance ID)
5V444H5WIC
REMIFENTANIL HYDROCHLORIDE
RxCUI 236540
Orange Book
A210594
APAPAP
DailyMed SPL labels
1 version tracked
FDA shortage
Currently in shortage
Remifentanil Hydrochloride Injection
Raw payload (JSON)
{
"unii": {
"unii": "5V444H5WIC",
"rxcui": "236540",
"inchikey": "WFBMIPUMYUHANP-UHFFFAOYSA-N",
"display_name": "REMIFENTANIL HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"5b8025d2-3424-477b-9cff-3990a98c2a65": {
"match": "brand_token",
"title": "REMIFENTANIL HYDROCHLORIDE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [FRESENIUS KABI USA, LLC]",
"spl_version": "3",
"published_date": "2025-03-10"
}
},
"productid": "0143-9392_5c5e498b-d829-4f78-bcca-466631014767",
"productndc": "0143-9392",
"dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"orange_book": {
"appl_no": "210594",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 1MG BASE/VIAL",
"product_no": "001",
"approval_date": "Oct 13, 2020"
},
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 2MG BASE/VIAL",
"product_no": "002",
"approval_date": "Oct 13, 2020"
},
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 5MG BASE/VIAL",
"product_no": "003",
"approval_date": "Oct 13, 2020"
}
],
"appl_type": "A"
},
"dea_schedule": "CII",
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "REMIFENTANIL HYDROCHLORIDE",
"shortage_reason": "Remifentanil Hydrochloride Injection",
"shortage_status": "current",
"proprietary_name": "REMIFENTANIL HYDROCHLORIDE",
"active_ingred_unit": "mg/2mL",
"application_number": "ANDA210594",
"marketing_category": "ANDA",
"nonproprietary_name": "REMIFENTANIL HYDROCHLORIDE",
"start_marketing_date": "20210515",
"active_numerator_strength": "2"
}Related drugs
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