United States · FDA National Drug Code directory

Survanta

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
0074-1040_6ff1e6a7-1578-4e78-b34f-eb204b23554c
Product NDC
0074-1040
Form
SUSPENSION
Composition / generic term
Beractant
Labeler
AbbVie Inc.
Marketing category
BLA
Marketing start / end (source format)
19910701
Source listing expiry
20261231

Source-listed ingredients

  • BERACTANT — 25 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL, SINGLE-USE in 1 CARTON (0074-1040-04) / 4 mL in 1 VIAL, SINGLE-USE · 0074-1040-04
  • 1 VIAL, SINGLE-USE in 1 CARTON (0074-1040-08) / 8 mL in 1 VIAL, SINGLE-USE · 0074-1040-08

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →