PANADOL

This brand name is authorized in Australia, Cyprus, Estonia, Finland, Hong Kong, Croatia, Ireland, Lithuania, Malta, Netherlands, New Zealand, Poland, Romania, Singapore, Tunisia, Turkey, United Kingdom

Active ingredients

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

1	Paracetamol UNII 362O9ITL9D - ACETAMINOPHEN
	Paracetamol is a medication used to treat pain and fever. It does appear to selectively inhibit COX activities in the brain, which may contribute to its ability to treat fever and pain.
	Read more about Paracetamol

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
PANADOL ORIGINAL Tablet	MPI, EU: SmPC	Medicines & Healthcare Products Regulatory Agency (GB)
PANADOL BABY Oral suspension	MPI, EU: SmPC	Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

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

ATC Group		Classification
N02BE01	Paracetamol	N Nervous system → N02 Analgesics → N02B Other analgesics and antipyretics → N02BE Anilides
Discover more medicines within N02BE01

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
AU	Pharmaceutical Benefits Scheme	12210P
EE	Ravimiamet	1009123, 1009145, 1076116, 1076127, 1076138, 1076149, 1076150, 1076161, 1076172, 1076183, 1076194, 1434787, 1434798, 1434800, 1434811, 1496033, 1496044, 1496055, 1496066, 1496077, 1496088, 1496099, 1496101, 1496112, 1496123, 1496134, 1496145, 1496156, 1496167, 1496178, 1531808, 1531819, 1531820, 1531842, 1531853
FI	Lääkealan turvallisuus- ja kehittämiskeskus	004524, 008259, 049134, 057965, 070745, 108221, 134353, 383992, 397302, 405069, 412630, 449174, 492793, 502182, 502735, 503831, 519580, 533406, 583638
GB	Medicines & Healthcare Products Regulatory Agency	149726, 149727, 18571, 325205, 46231
HK	Department of Health Drug Office	02280, 27104, 27105, 31209, 40505, 49376, 49789, 51314, 51316, 51472, 52665, 52683, 52694, 52933, 53362, 53813, 59436
HR	Agencija za lijekove i medicinske proizvode	HR-H-686856862, HR-H-772733493
LT	Valstybinė vaistų kontrolės tarnyba	1007942, 1007943, 1008529, 1008530, 1016505, 1056329, 1056330, 1056331, 1056332, 1061394, 1061395, 1063045, 1063046, 1063047, 1063048, 1063049, 1066418, 1066419, 1066420, 1070098, 1070099, 1070100, 1082881
MT	Medicines Authority	AA1177/00501, AA908/09101, MA1177/00503, MA1177/00504, MA460/00302, MA460/00303, PI274/01201A
NL	Z-Index G-Standaard, PRK	18120, 19720, 48267, 56006, 81442
NZ	Medicines and Medical Devices Safety Authority	10741, 11170, 11303, 12979, 12981, 13717, 14141, 14212, 15103, 15104, 21609, 21610, 236, 247, 8657
PL	Rejestru Produktów Leczniczych	100051046, 100051081, 100051098, 100110211, 100182854, 100282640, 100301431
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W64145002, W64145003, W64145004, W64146001, W64146002, W64146003, W64146004, W64146005, W64146006, W64146007, W64146008, W64146009, W64146010, W64146011, W64146012, W64146013, W64146014, W64146015, W64146016, W64146017, W64146018
SG	Health Sciences Authority	05919P, 05921P, 05922P, 07404P, 08739P, 10855P, 11734P, 11987P, 12406P, 13031P, 14699P
TN	Direction de la Pharmacie et du Médicament	9253191, 9253192, 9253193H, 9253194
TR	İlaç ve Tıbbi Cihaz Kurumu	8681291090035, 8681291090530, 8699522285945