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Tapentadol 75mg tablets are film-coated oral tablets containing Tapentadol hydrochloride as the active pharmaceutical ingredient, formulated for moderate to severe pain management. Each tablet is manufactured to precise pharmaceutical standards, with the API concentration confirmed at 75mg per unit. The product is designed for oral administration and is supplied in blister packs for hospital and wholesale distribution channels.
The tablets are produced under GMP-certified conditions, ensuring compliance with international pharmaceutical manufacturing standards. Tapentadol, as a centrally acting opioid analgesic, is classified under controlled substances regulations, requiring DEA scheduling compliance for import and export. The film coating provides stability and ease of swallowing, with typical dissolution profiles meeting USP or EP standards for immediate-release solid dosage forms.
This medication is primarily sourced by hospitals, pain management clinics, and pharmaceutical distributors for patient care. International trade requires a valid wholesale pharmaceutical license, and buyers must confirm regulatory compliance for their jurisdiction. The product is commonly exported from India, a major hub for generic pharmaceutical manufacturing, with logistics tailored to temperature-controlled shipping for stability.
| Active Pharmaceutical Ingredient | Tapentadol hydrochloride |
| Strength per tablet | 75mg |
| Formulation | Film-coated oral tablet |
| Packaging | Blister packs |
| Manufacturing Standard | GMP-certified |
| Regulatory Classification | Controlled substance (DEA scheduling required) |
| Dissolution Standard | Typical USP or EP compliance for immediate-release tablets |
| Storage Temperature | Standard 15-25°C, protect from moisture |
| Shelf Life | Typical 24-36 months under standard storage conditions |
| Primary Use | Moderate to severe pain management |
The supplier operates from Sindhudurg, India, with a focus on the wholesale distribution of pharmaceutical products. The listing does not provide additional details on company history, scale, or specific certifications beyond the GMP-compliant manufacturing reference for the product. Buyers should verify the supplier’s licensing and export capabilities directly before proceeding with orders.
This supplier specializes in controlled substance medications, including opioid analgesics like Tapentadol. The profile indicates an organic tier classification, but no response rate or average response time is available, suggesting limited engagement metrics. For procurement, buyers must ensure the supplier holds the necessary pharmaceutical export licenses and adheres to international trade regulations for controlled substances.
Tapentadol 75mg tablets are a prescription opioid analgesic for moderate to severe pain management. Supplied as film-coated oral tablets containing Tapentadol hydrochloride as the active pharmaceutical ingredient (API), this product is sourced from GMP-certified pharmaceutical manufacturers. Widely traded internationally for hospital procurement and pharmaceutical distribution networks, Tapentadol 75mg requires DEA scheduling compliance and a valid wholesale pharmaceutical license for import/export transactions.
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| 企业类型 | Supplier |
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| Main Products | View Products Tab |
| Major Markets | Global |
| 响应时间 | <4h |
| 响应率 | Contact Supplier |
Sourcing Tapentadol 75mg Tablets from Buy tapentadol 100mg online in USA - India Import Guide
Before ordering Tapentadol 75mg tablets, verify the supplier’s GMP certification and controlled substance export licenses. Confirm that the product meets the regulatory requirements of your destination country, particularly DEA scheduling for the USA. Request a Certificate of Analysis (CoA) to validate the API concentration and purity of the batch.
Logistics for this product require temperature-controlled shipping to maintain stability, as Tapentadol tablets are sensitive to moisture and extreme temperatures. Confirm the Incoterms (e.g., FOB or CIF) with the supplier and ensure the packaging complies with IATA or other relevant shipping regulations for pharmaceuticals. Lead times may vary, so request a confirmed delivery schedule in writing.
Quality checks should include visual inspection of the blister packs for integrity and labeling compliance. Request third-party laboratory testing for dissolution rates, API content, and impurity profiles to ensure the product meets USP or EP standards. Documentation such as the CoA, GMP certificate, and controlled substance permits must accompany the shipment for customs clearance.
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