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| Material | Active Pharmaceutical Ingredient Tapentadol Hydrochloride (Synthetic Opioid) |
| Dosage Forms | Tapentadol 100 mg immediate‑release tablets; Aspadol 50 mg immediate‑release tablets; Aspadol 150 mg and 200 mg extended‑release tablets |
| Schedule | Schedule II controlled substance (DEA) |
| Typical Tablet Weight | typical 220 mg per tablet |
| Typical Hardness | typical 8 - 10 kp |
| Typical Disintegration Time | typical ≤15 minutes |
| Packaging | typical blister pack of 10 tablets per strip, 10 strips per carton |
| Storage Condition | typical 20 - 25 °C, protected from light and moisture |
| Shipping Terms | FOB or CIF as offered by supplier |
| Payment Terms | L/C or T/T as indicated by supplier |
Safe Health Mart - Buy Medicines Online is registered at 6670 Villa Sonrisa Dr 222, Boca Raton, FL, United States. The platform classifies the supplier in the organic tier and assigns a harbour trust tier, indicating that the business has passed basic verification checks. No response rate or average response time is recorded in the listing, which suggests that the supplier has not yet engaged in trade conversations on the marketplace. The company advertises wholesale distribution of prescription‑only medicines, focusing on controlled‑substance compliance.
According to the listing, the supplier does not disclose specific certifications, production capacity or client references, so importers should request copies of the DEA registration, GMP certificates and batch analysis reports before committing to a purchase. The lack of detailed operational data means that due diligence must include verification of the supplier’s licence to export Schedule II opioids. All communications should be conducted through documented channels to maintain a clear audit trail.
Tapentadol 100mg and Aspadol 50mg/ER 150mg/200mg are centrally-acting analgesic medications classified as Schedule II controlled substances, used for management of moderate to severe pain. Available in immediate-release and extended-release tablet formulations for wholesale pharmaceutical distribution. These products require valid prescription, licensed pharmaceutical handling, and comply with DEA/authority scheduling regulations for international trade and regulated medicine supply chains.
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Before placing an order, verify that the supplier holds a current DEA registration for exporting Schedule II opioids and that the product batches are accompanied by a valid Certificate of Analysis. Request a copy of the manufacturing licence and a recent GMP audit report to ensure compliance with international quality standards. Confirm that the product label includes the required controlled‑substance information and that the export licence matches the destination country's regulations.
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Arrange for a pre‑shipment inspection by an accredited third‑party laboratory to verify tablet potency, hardness and packaging integrity. Ensure that the supplier provides the full batch documentation, including the Certificate of Analysis, stability data and a Material Safety Data Sheet for the active ingredient. Maintaining these records will simplify customs clearance and support post‑import quality assurance for your pharmacy or hospital network.
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