Augmentin

Medicinal product

(Invented) name

Augmentin

Active substance (s)

Amoksicilinas/Klavulano rūgštis

Strength

875 mg/125 mg

Pharmaceutical form

plėvele dengtos tabletės

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

GlaxoSmithKline (Ireland) Limited , Airija

Date of authorisation

1998-04-30

Date of renewal

2015-01-27

Documents

3675 Pakuotės lapelis 875_125 2024 08 31.docx

3675 Augmentin 875_125 tab RPP 2024 08 31.docx

Stage

Perregistruotas

Controlled?

No

Controlled substance type

Legal basis

8(3)

Procedure number

DE/H/2868/002/MR

Marketing authorisation procedure

Savitarpio pripažinimo procedūra

Qualitative and quantitative composition

Vienoje tabletėje yra	1 vnt.
Amoksicilinas	875 mg
Klavulano rūgštis	125 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
6304	2259	1002259	lizdinė plokštelė	N14		Receptinis	LT/1/98/3675/006	Tiekiama	-	-	No	-	-	Download

Stadijos

Data	Stadija
2015-01-27	Perregistruotas
1998-04-30	Registruotas