Humatrope

Medicinal product

(Invented) name

Humatrope

Active substance (s)

Somatropinas

Strength

12 mg

Pharmaceutical form

milteliai ir tirpiklis injekciniam tirpalui

Route (s) of administration

leisti po oda

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

H01AC01, Somatropin

Marketing authorisation holder

Eli Lilly Nederland B.V., Nyderlandai

Date of authorisation

1997-04-09

Date of renewal

2010-06-15

Documents

2050 Humatrope milt inj PCS PL 2021 11 12.docx

2050 Pakuotės lapelis 2021 11 12.docx

Stage

Išregistruotas

Controlled?

No

Controlled substance type

Legal basis

8(3)

Procedure number

Marketing authorisation procedure

Nacionalinė procedūra

Qualitative and quantitative composition

Užtaise yra	1 vnt.
Somatropinas	12 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
6133	915	1000915	užtaisas	milteliai ir užpildytas švirkštas tirpiklio (3,15 ml) N1		Receptinis	LT/1/97/2050/002	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2022-12-29	Išregistruotas
2010-06-15	Perregistruotas
1997-04-09	Registruotas