Product Images Tramadol Hydrochloride

NuCare Pharmaceuticals, Inc. provides Tramadol Hydrochloride 300mg ER Tablets with LOT# 000000. The NDC for this drug is 68071-2732-03 and the manufacturer's reference number is 47335-861-83 with an expiry date of 00-00. It is crucial to keep this product out of reach of children and store it between 68-77°F. For more details on the ingredients, please refer to the manufacturer's label. Contact 1-800-FDA-1088 in case of any reported case of adverse reactions.*

Hydrochloride Extended-Release Tablets are indicated for the management of moderate to moderately severe chronic pain in adults who require around-the-clock treatment of their pain for an extended period of time. b. Tramadol IR Tablets are indicated for the management of pain in adults that is severe enough to require an opioid analgesic and when other treatments, such as non-opioid pain medicines or immediate-release opioid medicines, do not treat your pain well enough or you cannot tolerate them. Note: The text includes medication names, doses, and indications for use. It provides important information for healthcare professionals related to the use of tramadol.*

The text describes two different medications for pain relief: Tramadol Hydrochloride Extended-Release Tablets, 200 mg quaque die (once daily) and Tramadol IR (Immediate-Release) Tablets, 50 mg every 6 hours. The medication names are followed by some code or reference numbers, possibly for inventory or tracking purposes.*

This is a description of Tramadol Hydrochloride Extended-Release Tablets and a graph showing a study (015) for arthritis pain relief. The graph appears to show the percentage of patients achieving various levels of pain relief in response to the tablets, with different dosage levels indicated. There is no other information available in the text.*