NPRA Banner

               
Product Search   QUEST3+ System   Enquiries   Sitemap  

Part I, Section D : Label (Mock-Up) for Immediate Container, Outer Carton and Proposed Package Insert & PIL

Reference National Pharmacy Regulatory Agency (formally known as National Pharmaceutical Control Bureau):
Drug Registration Guidance Document (DRGD) - Appendix 9: Labelling Requirement

Section Attachment/Information

D1

Label (Mock-up) for Immediate Container
Please refer:

Appendix 9: 9.1.1 LABEL (MOCK-UP) FOR IMMEDIATE CONTAINER AND OUTER CARTON

D2

Label (Mock-up) for Outer Carton
Please refer:

Appendix 9: 9.1.1 LABEL (MOCK-UP) FOR IMMEDIATE CONTAINER AND OUTER CARTON

D3

Proposed Package Insert
Please refer:
Appendix 9: 9.1.2 PROPOSED PACKAGE INSERT

D4

Patient Information Leaflet (PIL) / RisalahMaklumat Ubat Pesakit (RiMUP)
Please refer:

  1. DirektifPenguatkuasaanKeperluanMengemukakanRisalahMaklumat Ubat untukPengguna (RiMUP) Bil. 5 Year 2011 Bil (15) dlm BPFK/PPP/01/03 Jld 1
  2. Garispanduan Pelaksanaan Risalah Maklumat Ubat untukPengguna (RiMUP)

D5

Label (Mock-up) for Diluent
Please provide label (mockup) for diluent.

 

National Pharmaceutical Regulatory Agency (NPRA)

Lot 36, Jalan Universiti (Jalan Prof Diraja Ungku Aziz), 46200 Petaling Jaya, Selangor, Malaysia.

  • Phone: +603-7883 5400

 

 

DISCLAIMER

The Government of Malaysia and the National Pharmaceutical Regulatory Agency are not responsible for any loss or damage caused by the usage of any information obtained from this website.

Site Last Modified

  • Last Modified: Thursday 31 October 2024, 08:00:16.

Search

Main Menu English