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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

  • ndc11
    0074104004
    1 VIAL, SINGLE-USE in 1 CARTON (0074-1040-04) / 4 mL in 1 VIAL, SINGLE-USE
  • ndc11
    0074104008
    1 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"
}

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