United States · FDA National Drug Code directory
Propofol Injectable Emulsion
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
- 43598-265_b4a9147e-dfe3-229a-d8d7-6a84e6449f15
- Product NDC
- 43598-265
- Form
- INJECTION, EMULSION
- Composition / generic term
- Propofol Injectable Emulsion
- Labeler
- Dr. Reddy's Laboratories, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181115
- Source listing expiry
- 20261231
Source-listed ingredients
- PROPOFOL — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL in 1 CARTON (43598-265-25) / 20 mL in 1 VIAL (43598-265-20) · 43598-265-25
- 10 VIAL in 1 CARTON (43598-265-58) / 20 mL in 1 VIAL (43598-265-20) · 43598-265-58
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 →