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In pharmaceutical practice, tablets of this strength are produced to pharmaceutical‑grade standards, with typical tablet hardness of 5 - 8 kp and a dissolution rate exceeding 85 % within 30 minutes. The formulation follows common excipient blends such as microcrystalline cellulose and lactose, providing consistent tablet integrity. Export‑quality packaging is used to protect product integrity during transit. The tablets are designed for rapid absorption to deliver immediate and sustained pain relief.
Typical end‑users include hospitals, outpatient clinics and pain‑management centres that require reliable supply of moderate to severe pain medication. The supplier indicates flexible minimum order quantities and offers FOB or CIF shipping terms, though exact MOQ and lead time must be confirmed directly. Buyers should verify FDA compliance and request a certificate of analysis before import.
| Active Ingredient | Tapentadol 100 mg per tablet |
| Dosage Form | Oral tablet |
| Tablet Strength | 100 mg |
| Excipients | Standard pharmaceutical excipients (e.g., microcrystalline cellulose, lactose) typical |
| Tablet Hardness | typical 5 - 8 kp |
| Dissolution | typical >85 % in 30 min |
| Packaging | Export‑quality bulk packaging |
| Storage Condition | typical 20 - 25 °C, protected from moisture |
| Shelf Life | typical 24 months |
| Regulatory Compliance | FDA compliance |

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The current listing focuses on Noosanta 100 mg tapentadol tablets, positioned for pharmaceutical distributors and healthcare procurement specialists. No details on production capacity, exact minimum order quantity or lead‑time are disclosed, so prospective buyers should request this information from the supplier before placing an order.
Noosanta 100mg Tapentadol Tablets are a prescription analgesic for managing moderate to severe pain. This pharmaceutical preparation contains 100mg of tapentadol per tablet, formulated for oral administration. Ideal for pharmaceutical distributors and healthcare procurement specialists seeking bulk pain management medications. Meets pharmaceutical grade standards suitable for international pharmaceutical trade and distribution networks. Export-quality packaging ensures product integrity 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 placing an order, importers should confirm the product’s regulatory status by requesting the current FDA registration and a full certificate of analysis. Verify that the batch number, manufacturing date and expiry date are clearly indicated on the packaging documentation. It is also advisable to ask for a sample batch to assess tablet hardness and dissolution performance against the typical values provided.
Discuss shipping logistics early, specifying whether FOB or CIF terms will apply and confirming the port of loading in the United States. Since the supplier’s response metrics are not recorded, negotiate clear lead‑time expectations and agree on payment conditions such as a letter of credit or advance payment. Ensure that freight forwarders are aware of any temperature‑controlled requirements for pharmaceutical shipments.
Arrange for a third‑party quality inspection before loading, focusing on tablet hardness, dissolution rate and visual integrity. Request the supplier’s manufacturing batch record, stability data and any available GMP certificates to substantiate quality claims. Retain all inspection reports and certificates for customs clearance and post‑import quality assurance.
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