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RH057

WHO Product ID
RH057
Status
Prequalified
INN, dosage form and strength
Levonorgestrel Tablet, Film-coated 0.03mg
Date of prequalification
Basis of listing
Prequalification - Full
Therapeutic area
Reproductive health
Type
Finished Pharmaceutical Product
Dosage form
Tablet, Film-coated
Applicant organization
Senador Laboratories Private Limited
Plot 2B & 2C, Biotech Park, Phase II, Lalgadi Malakpet, Medchal Malkajgiri
Hyderabad,
Telangana
500101
India
Packaging details and storage conditions
Packaging Type
Blister, Alu/PVC/PVdC
Configuration
28x3, 35x3
Shelf life (months)
36
Storage conditions
Do not store above 30°C, protect from light
API Manufacturing Site(s)
By Organization
By Active Ingredient
Bayer AG
Bergkamen Plant, Ernst Schering Strasse 14
Bergkamen,
59192
Germany
Levonorgestrel
Industriale Chimica S.R.L
E. H. Grieg 13, Saronno
Varese,
21047
Italy
Levonorgestrel
FPP Manufacturing Site(s)
Senador Laboratories Private Limited
Plot No 20 & 21, Pharmez Sarkhej-Bavla National Highway No. 8A, Near Village Matoda, Taluka: Sanad
Dist. Ahmedabad,
Gujarat
382 213
India
WHO Public Assessment Reports


Part 1 - Abstract
Part 2a - All accepted presentations
Part 2b - Visual appearance of the product
Part 3 - WHO-PQ recommended patient information leaflet*
Part 4 - WHO-PQ recommended summary of product characteristics*
Part 5 - Label
Part 6 - Discussion (status at the time of prequalification)
Part 7 - Steps before Prequalification
Part 8 - Steps following Prequalification (from 01 March 2014, only changes to the published information are included)

* This summary of product characteristics/patient information leaflet focus on uses of the medicine covered by WHO Prequalification Team - Medicines. The recommendations for use are based on WHO guidelines and on information from stringent regulatory authorities (term to be revised). The medicine may be authorised for additional or different uses by national medicines regulatory authorities. 

Samples of the artworks of the SPC/PIL/labelling have not been submitted. Therefore, control of compliance with WHOPAR guidelines (contents and format) has not been possible.

Part 1 , Part 2a , Part 2b , Part 3 , Part 4 , Part 5 , Part 6 , Part 7 , Part 8

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