PROSTIN E2

This brand name is authorized in Austria, Canada, Cyprus, Hong Kong, Croatia, Ireland, Israel, Malta, Netherlands, New Zealand, Singapore, United Kingdom, United States

Active ingredients

The drug PROSTIN E2 contains one active pharmaceutical ingredient (API):

1 Dinoprostone
UNII K7Q1JQR04M - DINOPROSTONE
Read about Dinoprostone

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
PROSTIN E2 Concentrate for solution for infusion Medicines & Healthcare Products Regulatory Agency (GB) MPI, EU: SmPC
PROSTIN E2 Vaginal tablet Medicines & Healthcare Products Regulatory Agency (GB) MPI, EU: SmPC

Medicine classification

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

ATC code Group title Classification
G02AD02 Dinoprostone G Genito urinary system and sex hormones → G02 Other gynecologicals → G02A Oxytocics → G02AD Prostaglandins
Discover more medicines within G02AD02
G04BE01 Alprostadil G Genito urinary system and sex hormones → G04 Urologicals → G04B Other urologicals, incl. antispasmodics → G04BE Drugs used in erectile dysfunction
Discover more medicines within G04BE01

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: CA Health Products and Food Branch Identifier(s): 00400688, 01919679, 01919687
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 204712, 44073, 44088, 44103, 47549, 47552
Country: HK Department of Health Drug Office Identifier(s): 00443, 14469, 19734
Country: HR Agencija za lijekove i medicinske proizvode Identifier(s): HR-H-721133137
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 8924, 8926, 8927, 8928
Country: MT Medicines Authority Identifier(s): AA565/55404, MA505/02202, MA505/02203
Country: NL Z-Index G-Standaard Identifier(s): 14043513, 14043521
Country: NL Z-Index G-Standaard, PRK Identifier(s): 32301, 32328
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 2488, 2489
Country: SG Health Sciences Authority Identifier(s): 02520P
Country: US FDA, National Drug Code Identifier(s): 0009-0827

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