PREPIDIL

This brand name is authorized in United States. It is also authorized in Austria, Canada, Croatia, France, Netherlands, Poland, Tunisia.

Active ingredients

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

1	Dinoprostone UNII K7Q1JQR04M - DINOPROSTONE
	Read more about Dinoprostone

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
PREPIDIL Gel	MPI, US: SPL/Old	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	00860786
FR	Base de données publique des médicaments	64421236
HR	Agencija za lijekove i medicinske proizvode	HR-H-599786838
NL	Z-Index G-Standaard	14043491
NL	Z-Index G-Standaard, PRK	71943
PL	Rejestru Produktów Leczniczych	100054866
TN	Direction de la Pharmacie et du Médicament	4133011H
US	FDA, National Drug Code	0009-3359