PREDNISOLONE Polfa

Medicinal product

(Invented) name

PREDNISOLONE Polfa

Active substance (s)

Prednizolonas

Strength

5 mg

Pharmaceutical form

tabletės

Route (s) of administration

vartoti per burną

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

H02AB06, Prednisolone

Marketing authorisation holder

Adamed Pharma S.A., Lenkija

Date of authorisation

1995-10-04

Date of renewal

2011-12-21

Documents

2752 Pakuotės lapelis 2021_06_18.docx

2752 PREDNISOLONE Polfa 5mg tab PCS PL 2021_06_18.docx

Stage

Išregistruotas

Controlled?

No

Controlled substance type

Legal basis

10a

Procedure number

Marketing authorisation procedure

Nacionalinė procedūra

Qualitative and quantitative composition

Tabletėje yra	1 vnt.
Prednizolonas	5 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
1247	1604	1001604	buteliukas	N30		Receptinis	LT/1/95/2752/001	Netiekiama	-	-	No	-	-
66359	80884	1080884	lizdinė plokštelė	N20		Receptinis	LT/1/95/2752/002	Netiekiama	-	-	No	-	-	Download

Stadijos

Data	Stadija
2023-07-07	Išregistruotas
2011-12-21	Perregistruotas
1995-10-04	Registruotas