United States · FDA National Drug Code directory
propofol
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
- 16714-690_d7b2f7ed-e91e-430a-bab2-a9533b90e8b9
- Product NDC
- 16714-690
- Form
- INJECTION, EMULSION
- Composition / generic term
- propofol
- Labeler
- NorthStar Rx LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220701
- Source listing expiry
- 20261231
Source-listed ingredients
- PROPOFOL — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 CARTON (16714-690-10) / 100 mL in 1 VIAL (16714-690-01) · 16714-690-10
Source and coverage
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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.
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