United States · FDA National Drug Code directory
Sevoflurane
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
- 0527-6123_f3d34dea-e901-46b9-80f8-b314ca57020c
- Product NDC
- 0527-6123
- Form
- LIQUID
- Composition / generic term
- Sevoflurane
- Labeler
- Lannett Company, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230818
- Source listing expiry
- 20261231
Source-listed ingredients
- SEVOFLURANE — 250 mL/250mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, GLASS in 1 CARTON (0527-6123-74) / 250 mL in 1 BOTTLE, GLASS · 0527-6123-74
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 →