CERVIDIL

This brand name is authorized in United States. It is also authorized in Canada, New Zealand, Poland, Singapore.

Active ingredients

The drug CERVIDIL contains one active pharmaceutical ingredient (API):

1
UNII K7Q1JQR04M - DINOPROSTONE
 
Read more about Dinoprostone

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 CERVIDIL Vaginal insert MPI, US: SPL/PLR FDA, National Drug Code (US)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
G02AD02 Dinoprostone G Genito urinary system and sex hormones → G02 Other gynecologicals → G02A Oxytocics → G02AD Prostaglandins
Discover more medicines within G02AD02

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
CA Health Products and Food Branch 02231047
NZ Medicines and Medical Devices Safety Authority 9951
PL Rejestru Produktów Leczniczych 100404540
SG Health Sciences Authority 13982P
US FDA, National Drug Code 55566-2800

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