Agriculture›
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Construction & real estate›💡Electronic & Electrical›🍎Food & Beverages›🛋️Home furnishing & supplies›⚗️Industrial goods & chemical›🪨Minerals & metals›📦Miscellaneous›
Agriculture›
Apparel and fashion accessories›
Construction & real estate›💡Electronic & Electrical›🍎Food & Beverages›🛋️Home furnishing & supplies›⚗️Industrial goods & chemical›🪨Minerals & metals›📦Miscellaneous›The product offered is the active pharmaceutical ingredient Mifepristone, marketed under the name RU‑486. The supplier lists the material as Mifepristone, located in Ranchi with a mailing address at 411 Lafayette St, Cadiz Kentucky 42211, United States. The supplier tier is recorded as organic and the trust tier as voyage, while the response rate is shown as 0.00 with no average response time recorded. The listing notes that the substance belongs to the Fluorspar chemical family because its base compound is calcium fluoride (CaF2).
Mifepristone is a steroidal anti‑progesterone agent used in medically supervised termination procedures. In the pharmaceutical market the ingredient is typically supplied at a purity of 99 % or higher and is manufactured under Good Manufacturing Practice (GMP) standards. Typical assay values range from 99.5 % to 101 %, moisture content is kept below 0.5 % and the product is stored in amber glass vials at controlled room temperature to protect against light degradation. The compound is classified as a prescription drug and requires a valid import licence and a certificate of analysis for legal distribution in the United States.
Buyers such as hospitals, clinics and licensed pharmacies purchase Mifepristone for inclusion in approved treatment protocols. Importers must verify that the supplier holds the necessary authorisations from the FDA and that the shipment complies with all relevant drug‑control regulations. Trade terms should include confirmation of the certificate of analysis, packaging specifications, and agreed Incoterms before shipment. Because the listing does not disclose minimum order quantities, payment schedules or lead times, interested parties should contact the supplier directly to confirm those details.
| Material | Mifepristone |
| Chemical classification | Steroidal anti‑progesterone (RU‑486) |
| Purity (typical) | ≥99% |
| Assay (typical) | 99.5‑101% |
| Storage condition (typical) | 15‑30 °C, protected from light |
| Packaging (typical) | Amber glass vials, 100 mg per vial |
| Shelf life (typical) | 24 months at 25 °C |
| Regulatory status (typical) | Prescription drug, FDA‑approved active pharmaceutical ingredient |
| Supplier city | Ranchi |
| Supplier address | 411 Lafayette St, Cadiz Kentucky 42211, USA |
Buy oxycodone 30 mg tablets online USA is listed with an organic tier and a voyage trust tier, indicating a self‑declared commitment to sustainable sourcing. The profile shows a zero percent response rate and no average response time, suggesting that the supplier has not yet engaged in buyer communications on the platform. The address given places the business in Cadiz, Kentucky, while the city field mentions Ranchi, which may reflect a broader operational footprint.
The supplier’s only product description states that they sell legal Mifepristone in the United States and direct buyers to a legal website for order placement. No further corporate history, employee numbers or client references are provided, and the listing does not include any certified quality management system documentation. Prospective importers should therefore request verification of the supplier’s FDA registration and any third‑party audit reports before proceeding.
Mifepristone (also known as RU-486) is a steroidal anti-progesterone agent used in medical termination procedures. As a pharmaceutical active ingredient, it requires proper regulatory authorization for import and distribution. This product is related to the Fluorspar category due to its chemical classification; CaF2 (calcium fluoride) is the base compound. Trade in pharmaceutical substances is strictly regulated by national health authorities including the FDA, and all transactions must comply with applicable drug import and distribution laws in the destination jurisdiction.
| 企业类型 | Supplier |
| 成立年份 | Contact Supplier |
| Employees | Contact Supplier |
| Annual Revenue | Contact Supplier |
| Main Products | View Products Tab |
| Major Markets | Global |
| 响应时间 | <4h |
| 响应率 | Contact Supplier |
Before placing an order, verify that the supplier holds a current FDA registration and can provide a full certificate of analysis for each batch. Request documentation of the manufacturing GMP compliance and confirm that the product is classified as a prescription drug in the destination market. This verification helps avoid customs delays and ensures regulatory conformity.
Logistics for pharmaceutical active ingredients typically use air freight or temperature‑controlled sea containers under Incoterms such as CIP or DAP. Confirm the exact Incoterm, the expected lead time, and the payment schedule with the supplier before signing any contract. Because the listing does not disclose lead times, ask the supplier to provide a realistic shipping timeline based on their production capacity.
Upon arrival, conduct a visual inspection of the packaging, check batch numbers against the CoA, and verify that storage conditions were maintained during transit. Engage a qualified third‑party lab to re‑test purity and assay if required by your quality system. Retain all import licences, certificates and inspection reports as part of your compliance records.
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