Propofol Baxter

Medicinal product

(Invented) name

Propofol Baxter

Active substance (s)

Propofolis

Strength

20 mg/ml

Pharmaceutical form

injekcinė ar infuzinė emulsija

Route (s) of administration

leisti į veną

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

N01AX10, Propofol

Marketing authorisation holder

Baxter Holding B.V. , Nyderlandai

Date of authorisation

2009-05-19

Date of renewal

2019-03-04

Documents

1589 Pakuotės lapelis 20mg_ml 2022 01 10.docx

1589 Propofol Baxter 20mg_ml II PL 2022 01 10.docx

Stage

Išregistruotas

Controlled?

No

Controlled substance type

Legal basis

10(1)

Procedure number

NL/H/1268/002/MR

Marketing authorisation procedure

Savitarpio pripažinimo procedūra

Qualitative and quantitative composition

1 ml emulsijos yra	1 ml
Propofolis	20 mg

Packages

PAKID	NPAKID	NPAKID-7	Pack type	Pack size	Type of packaging	Proposed dispensing/classification	Marketing authorisation no.	Supply status	From	To	Package is in foreign language	From	To	Mock-up
30486	32947	1032947	flakonas	50 ml, N1		Receptinis	LT/1/09/1589/005	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2023-01-31	Išregistruotas
2019-03-04	Perregistruotas
2009-05-19	Registruotas