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Tapentadol 100 mg tablets are supplied for adult pain management and contain the active ingredient Tapentadol hydrochloride. Each tablet delivers a precise 100 mg dose of the non‑racemic molecule whose molecular formula is C14H23NO. The supplier lists both immediate‑release and extended‑release variants, allowing rapid onset or prolonged analgesia. The product is described as a potent analgesic with a dual mechanism targeting pain receptors and norepinephrine reuptake.
In pharmaceutical practice, Tapentadol tablets are typically produced with a hardness of 5 - 10 kp and a dissolution of at least 80 % within 30 minutes, meeting common pharmacopeial standards. Tablet weight commonly ranges around 200 mg and dimensions near 7 mm diameter, although exact figures are not supplied by the seller. The active ingredient is supplied as a hydrochloride salt, ensuring stability under standard storage conditions. No specific certifications are claimed by the supplier, so buyers should request any required GMP or FDA documentation.
The medication is used in hospitals, pain‑management clinics and outpatient pharmacies where prescription‑only analgesics are required. Trade terms such as minimum order quantity, packaging details and Incoterms are negotiable directly with the supplier. Importers should confirm secure packaging and shipping options to maintain product integrity during transit.
| Dosage per tablet | 100 mg |
| Formulation | Immediate‑release; Extended‑release (as listed) |
| Molecular formula | C14H23NO |
| Active ingredient | Tapentadol hydrochloride |
| Tablet weight | typical 200 mg |
| Tablet diameter | typical 7 mm |
| Hardness | typical 5 - 10 kp |
| Dissolution (30 min) | typical ≥80 % |
| Packaging | typical blister pack of 10 tablets |
| Storage condition | typical 15 - 30 °C |
The supplier is identified only by the web address https://tapentadol100mgonline.com/. It is classified as an imported tier with a harbor trust level on the platform, and its response rate is currently recorded as 0 %. No further corporate information is provided in the listing.
Because the listing does not disclose certifications, manufacturing capacity or years in operation, buyers should request these details before committing to purchase. The supplier states that products are shipped securely, but specific packaging formats are not enumerated.
| Business Type | Supplier |
| Year Established | Recently Joined |
| Employees | Contact Supplier |
| Annual Revenue | Contact Supplier |
| Main Products | View Products Tab |
| Major Markets | Global |
| Response Time | <4h |
| Response Rate | New Supplier |
Before placing an order, importers should verify the supplier’s corporate registration, trust tier and response history, and request proof of any manufacturing licences or regulatory approvals that cover Tapentadol. Because the listing does not provide these documents, a direct request for a GMP certificate, FDA registration number and a recent third‑party audit report is essential to assess product legitimacy.
Logistics considerations include confirming the preferred Incoterm, whether FOB or CIF, and clarifying the expected lead time for production and shipping. As the supplier does not publish lead‑time data, buyers must obtain a realistic schedule and ensure that the agreed shipping method can preserve tablet stability, especially if temperature‑controlled transport is required.
Quality assurance should involve arranging an independent inspection of the batch, reviewing the Certificate of Analysis, and checking that the tablets meet the specified hardness and dissolution criteria. Importers are advised to include clauses for random sampling and to retain documentation such as the batch number, manufacturing date and expiry date for traceability.
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