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United States · US · US:25021-676_5eb44748-b3d4-4d86-a172-9f03eb804671
pentobarbital sodium
Orange BookUNIISPLATC N05CA01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSagent Pharmaceuticals
CountryUS (United States)
ATC codeN05CA01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1125021676201 VIAL in 1 CARTON (25021-676-20) / 20 mL in 1 VIAL
- ndc1125021676501 VIAL in 1 CARTON (25021-676-50) / 50 mL in 1 VIAL
Annotations
UNII (FDA Substance ID)
NJJ0475N0S
PENTOBARBITAL SODIUM
RxCUI 203085
Orange Book
A206404
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "NJJ0475N0S",
"rxcui": "203085",
"inchikey": "QGMRQYFBGABWDR-UHFFFAOYSA-M",
"display_name": "PENTOBARBITAL SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAMUSCULAR; INTRAVENOUS",
"spl_meta": {
"d375b92a-baa1-4d63-9ad1-1467dcfde7d5": {
"match": "brand_token",
"title": "PENTOBARBITAL SODIUM INJECTION, SOLUTION [HIKMA PHARMACEUTICALS USA INC.]",
"spl_version": "5",
"published_date": "2026-03-06"
}
},
"productid": "25021-676_5eb44748-b3d4-4d86-a172-9f03eb804671",
"productndc": "25021-676",
"dosage_form": "INJECTION, SOLUTION",
"orange_book": {
"appl_no": "206404",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "50MG/ML",
"product_no": "001",
"approval_date": "May 23, 2016"
}
],
"appl_type": "A"
},
"dea_schedule": "CII",
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PENTOBARBITAL SODIUM",
"proprietary_name": "pentobarbital sodium",
"active_ingred_unit": "mg/mL",
"application_number": "ANDA206404",
"marketing_category": "ANDA",
"nonproprietary_name": "pentobarbital sodium",
"start_marketing_date": "20170419",
"active_numerator_strength": "50"
}Related drugs
Other records sharing ATC code N05CA01.
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