Ammonaps

Medicinal product

(Invented) name

Ammonaps

Active substance (s)

Natrio fenilbutiratas

Strength

500 mg

Pharmaceutical form

tabletės

Route (s) of administration

vartoti per burną

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

A16AX03, Sodium phenylbutyrate

Marketing authorisation holder

Immedica Pharma AB, Švedija

Date of authorisation

1999-12-08

Date of renewal

Documents

Search in EMA Europe

Stage

Registruotas

Controlled?

No

Controlled substance type

Legal basis

8(3)

Procedure number

Marketing authorisation procedure

Centrinė registracija

Qualitative and quantitative composition

Tablet	1 vnt.
Natrio fenilbutiratas	500 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
24727	27370	1027370	buteliukas	N250		Receptinis	EU/1/99/120/001	Netiekiama	-	-	No	-	-
24728	27371	1027371	buteliukas	N500		Receptinis	EU/1/99/120/002	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
1999-12-08	Registruotas