NDC 0641-6195 – Propofol

Propofol 10 mg/mL · Injection, Emulsion · Intravenous

Human Prescription Drug

Product NDC0641-6195

Product details

Brand name
Propofol
Generic name
Propofol
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Injection, Emulsion
Route
Intravenous
Marketing category
ANDA · ANDA074848
Marketed since
May 1, 2020
Listing expires
December 31, 2026
Pharmacologic class
General Anesthetic

Active ingredients

Uses, dosage, side effects and warnings for Propofol →

Package NDC codes (1)

Package NDCDescriptionSince
0641-6195-2020 VIAL, SINGLE-USE in 1 CARTON (0641-6195-20) / 50 mL in 1 VIAL, SINGLE-USE (0641-6195-01)May 1, 2020

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