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Tapentadol 200 mg tablets are listed as a centrally‑acting analgesic intended for moderate to severe pain. Each tablet delivers a precise 200 mg dose of the active pharmaceutical ingredient, classified as a Schedule II controlled substance in the source text. The product is described as being supplied by a manufacturer in India and intended for prescription‑only use in the United States market. The supplier indicates that the tablets require cold‑chain storage and tamper‑evident packaging during transit.
In the pharmaceutical industry, a 200 mg tablet typically weighs around 400 mg and measures approximately 8 mm in diameter, with a hardness of 6 - 12 kp and dissolution of at least 85 % within 30 minutes, aligning with common pharmacopeial expectations. While the listing does not provide exact tablet dimensions, these values represent standard specifications for high‑dose opioid analgesics. The material is described only as “Medical”, and no explicit formulation details such as release profile are given. Because no certifications are claimed, buyers should request GMP, FDA and DEA documentation to confirm regulatory compliance.
The medication is suitable for hospitals, surgical centres and outpatient clinics that manage acute or chronic pain under controlled‑substance regulations. Trade terms, including minimum order quantities, packaging options and Incoterms, are to be negotiated directly with the supplier. Prospective importers should verify that the supplier can provide secure, temperature‑controlled shipping and that all required import licences are in place.
| Dosage per tablet | 200 mg |
| Active ingredient | Tapentadol hydrochloride |
| Regulatory classification | Schedule II (to be confirmed) |
| Tablet weight | typical 400 mg |
| Tablet diameter | typical 8 mm |
| Hardness | typical 6 - 12 kp |
| Dissolution (30 min) | typical ≥85 % |
| Packaging | typical blister pack of 10 tablets |
| Storage condition | typical 2 - 8 °C (cold‑chain) |
| Shelf life | typical 24 months |
The supplier, listed as “Buy Aspadol 100Mg Online in USA”, operates from Mumbai City, India, with an address noted as New Yark. It is categorised on the platform as an organic tier supplier with a voyage trust level, and its response rate is currently recorded as 0 %.
The product listing does not disclose manufacturing licences, GMP certification or FDA approval, so importers should request these documents. No specific details about production capacity or years in business are provided.
Tapentadol 200mg is a centrally-acting analgesic used for managing moderate to severe pain, available by prescription only. As a Schedule II controlled substance, international trade requires DEA authorization, import licenses, and compliance with FDA and customs regulations. B2B buyers must hold valid pharmaceutical distribution licenses and ensure cold-chain storage and tamper-evident packaging during transit.
| 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 committing to purchase, importers should verify the supplier’s corporate registration, trust tier and response history, and request copies of manufacturing licences, GMP certificates and DEA authorisation that cover Tapentadol. Because the listing provides no such documentation, a direct request for these records is essential to confirm the product’s legality and quality.
Logistics planning should include confirming the preferred Incoterm, expected lead time and the availability of temperature‑controlled transport. As lead‑time details are not published, buyers must obtain a realistic schedule and ensure that the shipping method preserves the required 2 - 8 °C storage condition throughout the journey.
Quality control measures should involve arranging an independent inspection of the batch, reviewing the Certificate of Analysis and verifying 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 batch number, manufacturing date and expiry date for full traceability.
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