ULTRAM

This brand name is authorized in United States

Active ingredients

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

1 Tramadol UNII 9N7R477WCK - TRAMADOL HYDROCHLORIDE

Tramadol is a centrally acting opioid analgesic. It is a non selective pure agonist at μ-, δ- and κ-opioid receptors with a higher affinity for the μ-receptor. Other mechanisms which may contribute to its analgesic effect are inhibition of neuronal reuptake of noradrenaline and enhancement of serotonin release. Tramadol has an antitussive effect. In contrast to morphine, analgesic doses of tramadol over a wide range have no respiratory depressant effect. Read about Tramadol

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
ULTRAM Coated tablet	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
N02AX02	Tramadol	N Nervous system → N02 Analgesics → N02A Opioids → N02AX Other opioids
Discover more medicines within N02AX02

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
Country: US	FDA, National Drug Code	Identifier(s): 50458-659, 80425-0057, 80425-0058