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United States · US · US:0074-1040_6ff1e6a7-1578-4e78-b34f-eb204b23554c
Survanta
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAbbVie Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1100741040041 VIAL, SINGLE-USE in 1 CARTON (0074-1040-04) / 4 mL in 1 VIAL, SINGLE-USE
- ndc1100741040081 VIAL, SINGLE-USE in 1 CARTON (0074-1040-08) / 8 mL in 1 VIAL, SINGLE-USE
Annotations
UNII (FDA Substance ID)
S866O45PIG
BERACTANT
RxCUI 46967
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "S866O45PIG",
"rxcui": "46967",
"inchikey": null,
"display_name": "BERACTANT",
"substance_type": "mixture",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ENDOTRACHEAL",
"spl_meta": {
"7ef9e3a5-fc39-4ae1-0dad-6b47a1684635": {
"match": "brand_token",
"title": "SURVANTA (BERACTANT) SUSPENSION [ABBVIE INC.]",
"spl_version": "46",
"published_date": "2024-03-04"
}
},
"productid": "0074-1040_6ff1e6a7-1578-4e78-b34f-eb204b23554c",
"productndc": "0074-1040",
"dosage_form": "SUSPENSION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "BERACTANT",
"proprietary_name": "Survanta",
"active_ingred_unit": "mg/mL",
"application_number": "BLA020032",
"marketing_category": "BLA",
"nonproprietary_name": "Beractant",
"start_marketing_date": "19910701",
"active_numerator_strength": "25"
}Access this data programmatically
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