Product information
From Health Canada
Current status:
Cancelled Post Market
Current status date:
2006-08-17
Original market date: See footnote 1
1997-10-08
Product name:
PUREGON 50 I.U.
DIN:
02231655 Electronic product monograph is not available
Company:
ORGANON CANADA LTD LTEE
16750 Route Transcanadienne
Kirkland
Quebec
Canada
H9H 4M7
Class:
Human
Dosage form(s):
Powder For Solution , Liquid
Route(s) of administration:
Subcutaneous , Intramuscular
Number of active ingredient(s):
2
Schedule(s):
Schedule D , Prescription
American Hospital Formulary Service (AHFS): See footnote 3
68:18.00
Anatomical Therapeutic Chemical (ATC): See footnote 4
G03GA06 FOLLITROPIN BETA
Active ingredient group (AIG) number:See footnote5
0232900002
Active ingredient(s) | Strength |
---|---|
FOLLITROPIN BETA | 50 UNIT / KIT |
SODIUM CHLORIDE | 1 ML / KIT |