DIPROLENE

This brand name is authorized in Canada, France, Netherlands, New Zealand, Poland, United States

Active ingredients

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

1 Betamethasone
UNII 826Y60901U - BETAMETHASONE DIPROPIONATE

Betamethasone is a glucocorticoid which is about eight to ten times as active as prednisolone on a weight-for-weight basis. Betamethasone has anti-inflammatory, antipruritic, and vasoconstrictive properties.

Read about Betamethasone

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
DIPROLENE AF Cream FDA, National Drug Code (US) MPI, US: SPL/PLR

Medicine classification

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

ATC code Group title Classification
D07AC01 Betamethasone D Dermatologicals → D07 Corticosteroids, dermatological preparations → D07A Corticosteroids, plain → D07AC Corticosteroids, potent (group III)
Discover more medicines within D07AC01

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): 00629367
Country: FR Base de donnรฉes publique des mรฉdicaments Identifier(s): 69337589
Country: NL Z-Index G-Standaard Identifier(s): 12513040
Country: NL Z-Index G-Standaard, PRK Identifier(s): 79979
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 2154, 2159
Country: PL Rejestru Produktรณw Leczniczych Identifier(s): 100019427, 100382984, 100413450, 100426581
Country: US FDA, National Drug Code Identifier(s): 0085-0517, 0085-0575, 0085-0962

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