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Ambien 10mg contains zolpidem tartrate as its active ingredient, supplied as oral tablets for the short-term treatment of insomnia. Each tablet delivers a precise 10mg dose, formulated to act on GABA receptors to induce sedation and reduce sleep latency. This prescription medication is classified as a Schedule IV controlled substance, requiring strict adherence to regulatory frameworks for distribution and import.
The tablets are typically white, film-coated, and scored for ease of division, with standard dimensions of approximately 8-9mm in diameter and 3-4mm in thickness. Zolpidem tartrate is a non-benzodiazepine hypnotic, often preferred for its lower risk of dependence compared to traditional benzodiazepines. Standard pharmaceutical grade material meets USP or EP monograph specifications for purity, assay, and dissolution.
Ambien 10mg is primarily sourced by hospitals, pharmacies, and licensed healthcare distributors for dispensing to patients with documented insomnia. International trade requires FDA approval for the US market and DEA compliance for controlled substance handling. Buyers must confirm import permits, storage conditions (typically 20-25°C, protected from moisture), and cold chain requirements if applicable.
| Active Ingredient | Zolpidem tartrate |
| Dosage Strength | 10mg per tablet |
| Form | Oral tablet, film-coated |
| Tablet Dimensions | typical 8-9mm diameter, 3-4mm thickness |
| Colour | White |
| Scoring | Yes, for division |
| Pharmacological Class | Non-benzodiazepine hypnotic, Schedule IV controlled substance |
| Mechanism of Action | GABA-A receptor agonist |
| Storage Temperature | typical 20-25°C, protected from moisture |
| Standard Compliance | USP or EP monograph for purity, assay, dissolution |
The supplier operates from Sindhudurg, India, with a focus on pharmaceutical products for international trade. The profile indicates an organic tier classification, though response metrics such as rate and average hours are currently unavailable. This suggests a newer or less active presence in the marketplace, requiring direct outreach for verification of capabilities and reliability.
The business specialises in controlled substances and prescription medications, including Ambien 10mg. No additional details are provided regarding manufacturing certifications, facility audits, or export licences, which buyers must confirm independently. The absence of stated history, headcount, or client references underscores the need for due diligence before engaging in trade.
Ambien 10mg (zolpidem tartrate) is a prescription sleep aid medication used for the short-term treatment of insomnia. This pharmaceutical product is supplied as 10mg oral tablets intended for dispensing through licensed pharmacies and healthcare facilities. Suitable for import/export trade in the pharmaceutical sector, this Schedule IV controlled substance requires proper regulatory documentation including FDA approval and DEA scheduling compliance for international commerce.
| 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 ordering Ambien 10mg, verify the supplier’s export licence for controlled substances and confirm their compliance with FDA and DEA regulations for the US market. Request documentation such as certificates of analysis, manufacturing authorisations, and cold chain validation if applicable to ensure product integrity during transit.
Confirm logistics details including lead time, which may vary due to regulatory approvals and controlled substance handling requirements. Incoterms such as CIF or FOB should be clarified, along with preferred ports of entry and any restrictions on air freight due to the product’s classification. Payment terms must align with regulatory hold periods for controlled substances.
Conduct quality checks upon receipt, including visual inspection for tablet colour, scoring, and packaging integrity. Request third-party testing for assay and dissolution to confirm compliance with USP/EP standards. Ensure all import permits and customs declarations are accurate to avoid delays or seizures at the border.
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