PANDA NIGHT

This brand name is authorized in Nigeria.

Active ingredients

The drug PANDA NIGHT contains a combination of these active pharmaceutical ingredients (APIs):

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
2	Diphenhydramine UNII TC2D6JAD40 - DIPHENHYDRAMINE HYDROCHLORIDE
	Diphenhydramine is an ethanolamine-derivative antihistamine. It is an antihistamine with anticholinergic and marked sedative effects. It acts by inhibiting the effects on H1-receptors. Diphenhydramine is effective in reducing sleep onset (i.e., time to fall asleep) and increasing the depth and quality of sleep.
	Read more about Diphenhydramine

Packages

This drug has been approved in Nigeria as follows:

Identifier	Form	Presentation	Description	Approval
A4-9817	Tablet	Panda Night Caplets TAB 500 mg; 25 mg	90 Paracetamol BP & Diphenhydramine Hcl A4-9817 Panda Night Caplets Paracetamol BP:,Diphenhydramine Hcl:,Povidone Pvp K-:,Croscarmellose Sodium,Microcrystalline Cellulose,Isopropyl Alcohol,Prosolve Talc,Magnesium Stearate,Sepifilm (Hpmc),Titanium Dioxide,Fd&C Blue Analgesics Oral 500 mg,30,Micro 90 mg,500 mg25 mg, Tablet Over The Counter (Otc) Afrab Chem Limited Afrab Chem Limited Nigeria 01/03/2021 28/02/2026	01/03/2021

Medicine classification

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

ATC Group		Classification
N02BE51	Paracetamol, combinations excl. psycholeptics	N Nervous system → N02 Analgesics → N02B Other analgesics and antipyretics → N02BE Anilides
Discover more medicines within N02BE51

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
NG	Registered Drug Product Database	A4-9817