GRANPIDAM

This brand name is authorized in Austria, Cyprus, Germany, Estonia, Spain, Finland, France, Croatia, Ireland, Italy, Lithuania, Netherlands, Poland, Romania, United Kingdom

Active ingredients

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

1 Sildenafil UNII BW9B0ZE037 - SILDENAFIL CITRATE

Sildenafil is a potent and selective inhibitor of cyclic guanosine monophosphate (cGMP) specific phosphodiesterase type 5 (PDE5), the enzyme that is responsible for degradation of cGMP. Apart from the presence of this enzyme in the corpus cavernosum of the penis, PDE5 is also present in the pulmonary vasculature. Sildenafil, therefore, increases cGMP within pulmonary vascular smooth muscle cells resulting in relaxation. Read about Sildenafil

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
GRANPIDAM Film-coated tablet	European Medicines Agency (EU)	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
G04BE03	Sildenafil	G Genito urinary system and sex hormones → G04 Urologicals → G04B Other urologicals, incl. antispasmodics → G04BE Drugs used in erectile dysfunction
Discover more medicines within G04BE03

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
Country: DE	Bundesinstitut für Arzneimittel und Medizinprodukte	Identifier(s): 12528947, 12528976
Country: EE	Ravimiamet	Identifier(s): 1734117, 1734128, 1764345, 1861073, 1861084
Country: ES	Centro de información online de medicamentos de la AEMPS	Identifier(s): 1161137001
Country: FI	Lääkealan turvallisuus- ja kehittämiskeskus	Identifier(s): 102935, 176078
Country: FR	Base de données publique des médicaments	Identifier(s): 65835628
Country: GB	Medicines & Healthcare Products Regulatory Agency	Identifier(s): 349375
Country: IE	Health Products Regulatory Authority	Identifier(s): 88759
Country: IT	Agenzia del Farmaco	Identifier(s): 045184013, 045184049
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 1081621, 1081622, 1087477, 1087478, 1087479
Country: NL	Z-Index G-Standaard, PRK	Identifier(s): 80365
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100381855
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): W65670001, W65670002