Augmentin ES

Medicinal product

(Invented) name

Augmentin ES

Active substance (s)

Amoksicilinas/Klavulano rūgštis

Strength

600 mg/42,9 mg/5 ml

Pharmaceutical form

milteliai geriamajai suspensijai

Route (s) of administration

vartoti per burną

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

J01CR02, Amoxicillin and beta-lactamase inhibitor

Marketing authorisation holder

UAB GlaxoSmithKline Lietuva, Lietuva

Date of authorisation

2008-07-03

Date of renewal

2015-05-13

Documents

1191_1_4 Augmentin ES 600_42,9_5 milt susp RPP 180508.docx

Stage

Išregistruotas

Controlled?

No

Controlled substance type

Legal basis

8(3)

Procedure number

PT/H/0684/001/MR

Marketing authorisation procedure

Savitarpio pripažinimo procedūra

Qualitative and quantitative composition

5 ml suspensijos yra	5 ml
Amoksicilinas	600 mg
Klavulano rūgštis	42,9 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
17937	21696	1021696	buteliukas	50 ml, N1		Receptinis	LT/1/98/1191/001	Netiekiama	-	-	No	-	-
17938	21697	1021697	buteliukas	75 ml, N1		Receptinis	LT/1/98/1191/002	Netiekiama	-	-	No	-	-
17939	4909	1004909	buteliukas	100 ml, N1		Receptinis	LT/1/98/1191/003	Netiekiama	-	-	No	-	-
17940	21698	1021698	buteliukas	150 ml, N1		Receptinis	LT/1/98/1191/004	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2018-08-02	Išregistruotas
2015-05-13	Perregistruotas
2008-07-03	Registruotas