NDC 23155-345

propofol

Propofol

propofol is a Intravenous Injection, Emulsion in the Human Prescription Drug category. It is labeled and distributed by Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals Inc.. The primary component is Propofol.

• Product ID: 23155-345_220cee57-08ef-46c3-ad39-7636d28bca38
• NDC: 23155-345
• Product Type: Human Prescription Drug
• Proprietary Name: propofol
• Generic Name: Propofol
• Dosage Form: Injection, Emulsion
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2021-10-12
• Marketing Category: ANDA /
• Application Number: ANDA206408
• Labeler Name: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
• Substance Name: PROPOFOL
• Active Ingredient Strength: 10 mg/mL
• Pharm Classes: General Anesthesia [PE], General Anesthetic [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 23155-345-41

10 VIAL in 1 CARTON (23155-345-41) > 20 mL in 1 VIAL (23155-345-31)

• Marketing Start Date: 2021-10-12
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "propofol" or generic name "Propofol"

NDC	Brand Name	Generic Name
0069-0209	Propofol	Propofol
0069-0234	Propofol	Propofol
0069-0248	Propofol	Propofol
0404-9943	PROPOFOL	propofol
0409-4699	PROPOFOL	PROPOFOL
0409-6010	PROPOFOL	PROPOFOL
0591-2136	Propofol	Propofol
0641-6194	Propofol	Propofol
0641-6195	Propofol	Propofol
0641-6196	Propofol	Propofol
16714-528	propofol	propofol
16714-690	propofol	propofol
16714-977	propofol	propofol
23155-345	propofol	propofol
25021-608	propofol	propofol
50090-4569	Propofol	Propofol
51662-1293	PROPOFOL	PROPOFOL
51662-1470	PROPOFOL	PROPOFOL
51662-1471	PROPOFOL	PROPOFOL
52584-054	Propofol	Propofol
52584-098	PROPOFOL	propofol
52584-699	Propofol	Propofol
18124-027	Fresenius Propoven 2%	PROPOFOL