Tramadol Hydrochloride
Product Images NDC 68071-2329

NuCare Pharmaceuticals, Inc. produces Tramadol Hydrochloride extended-release tablets containing Tramadol Hydrochloride USP 300 mg. These tablets are for oral use only and can be habit-forming. Each tablet is circular and white/off-white with "LO12" imprinted on one side. The tablets are to be kept out of reach of children and stored at controlled temperatures between 59-86°F. The batch or lot number is 000000 and the expiration date is 00-00. The product number is P2224060 and the manufacturer's NDC for this product is 68180-695-06. The FDA should be contacted at 1-800-FDA-1088 for any side effects or product concerns. Note that the above description was generated with text which might contain errors.*

The given text describes a chart that shows the Tramadol Concentration (ng/mL) at different intervals of time (h). The chart depicts the concentration at various levels ranging from 50 to 350. It highlights the comparison between Tramadol Hydrochloride Extended-Release Tablets of 200mg and Tramadol Hydrochloride Tablets of 50mg.*

This is a chart showing the concentration of M1 in ng/mL over time (in hours) for two different medications containing Tramadol Hydrochloride. The first medication is Tramadol Hydrochloride Extended-Release Tablets with a dosage of 200 mg per day and the second medication is Tramadol Hydrochloride Tablets with a dosage of 50 mg every 6 hours.*

This is a graph showing the percentage of patients achieving various levels of response threshold for Tramadol Hydrochloride Extended-Release Tablets Study 015 for Arthritis Pain Intensity VAS Responder Analysis. It indicates the response thresholds as various percentages of improvement from baseline and the percentage of patients achieving that level of response for both the medication and placebo groups.*