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Ambien 12.5mg is supplied as a tablet that contains the active ingredient zolpidem, a prescription sedative‑hypnotic indicated for short‑term treatment of insomnia. The product is manufactured under strict quality standards in an FDA‑approved facility and is classified as a Schedule IV controlled substance, meaning it can only be shipped with valid prescription documentation. This medication is intended for hospital, clinic and pharmacy distribution where regulated handling is mandatory.
The tablet form is typical of oral hypnotics, with a usual tablet weight of about 150 mg and a hardness of 8‑10 kp to ensure mechanical stability. Industry practice requires a dissolution of at least 80 % within 30 minutes, and storage at a controlled temperature of 20‑25 °C to preserve potency. Common packaging for this dosage strength is a blister pack containing ten tablets, which aids in dose accuracy and protection from moisture.
Importers targeting the United States market should verify the supplier’s licensing, confirm that the shipment complies with cold‑chain requirements where applicable, and request a Certificate of Analysis for each batch. Trade terms such as FOB or CIF are typically offered, but exact lead times and minimum order quantities are not disclosed in the listing and should be confirmed directly with the supplier. Proper regulatory documentation, including an import licence and the prescription, must accompany the consignment to satisfy customs and health authority checks.
| Form | Tablet |
| Active Ingredient | Zolpidem |
| Dosage per Tablet | 12.5 mg |
| Schedule | IV (Controlled Substance) |
| Manufacturing Facility Standard | FDA‑approved |
| Typical Tablet Weight | typical 150 mg |
| Typical Hardness | typical 8‑10 kp |
| Typical Dissolution | typical ≥80 % in 30 min |
| Typical Storage Temperature | typical 20‑25 °C |
| Typical Packaging | typical blister pack of 10 tablets |

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The company’s profile does not provide additional historical or financial details. It presents itself as a source for pharmaceutical products such as Ambien 12.5 mg, emphasizing compliance with regulatory standards but does not disclose specific certifications, production capacities or client references.
Ambien 12.5mg is a prescription sedative-hypnotic medication indicated for the short-term treatment of insomnia. This pharmaceutical product contains zolpidem as its active ingredient and is manufactured under strict quality standards for hospital and pharmacy distribution. As a Schedule IV controlled substance, it requires valid prescription documentation for procurement. Widely traded in wholesale pharmaceutical supply chains, this product is relevant for importers and exporters operating in the healthcare and medical supply sector. Proper licensing, cold chain compliance, and regulatory documentation are essential for international trade of this medication.
| 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, confirm that the supplier holds a valid pharmaceutical licence, can provide a Certificate of Analysis for the specific batch, and is authorized to export Schedule IV substances to your destination. Request copies of manufacturing records and any relevant GMP certifications to ensure regulatory compliance.
Discuss logistics in detail: verify the Incoterm (FOB, CIF or others), confirm whether temperature‑controlled transport is needed, and agree on lead‑time expectations. Payment terms such as a confirmed Letter of Credit are common for controlled pharmaceuticals, but the exact arrangement should be agreed with the supplier.
Implement a quality assurance plan that includes third‑party inspection of tablet weight, hardness and dissolution prior to shipment. Ensure that labeling meets both source and destination regulatory requirements and retain all inspection reports and certificates for customs clearance and post‑import audits.
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