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Safe Health Mart offers Carisoprodol tablets in two strengths, 350 mg and 500 mg, formulated for short‑term relief of acute musculoskeletal pain. Each tablet contains the active pharmaceutical ingredient Carisoprodol (N‑isopropyl‑2‑methyl‑2‑propyl‑1,3‑propanediol dicarbamate) as described in the supplier data. The product complies with standard pharmaceutical specifications for assay, dissolution and purity, as required for Schedule IV controlled substances. The listing indicates United States origin and domestic shipping.
Carisoprodol is classified as a centrally acting muscle relaxant and is manufactured by licensed pharmaceutical facilities that follow current Good Manufacturing Practice. Typical tablets in this class weigh around 0.65 g, exhibit a hardness of about 7 kp and dissolve at least 85 % within 30 minutes under USP conditions. Common industry packaging consists of 100 tablets per HDPE bottle, stored at 20‑25 °C away from moisture. These typical parameters help buyers assess compatibility with their quality control protocols.
The tablets are primarily used by hospitals, clinics and rehabilitation centres that treat muscle spasm and pain. Importers should arrange for DEA‑authorized licensing and provide appropriate documentation for controlled‑substance shipment. Trade terms frequently include flexible minimum order quantities, payment by irrevocable Letter of Credit or Telegraphic Transfer, and US‑to‑US freight on a door‑to‑door basis. Buyers are advised to confirm lead times and Incoterms directly with the supplier before finalising the order.
| Dosage strength (350 mg tablet) | 350 mg |
| Dosage strength (500 mg tablet) | 500 mg |
| Active pharmaceutical ingredient | Carisoprodol (N‑isopropyl‑2‑methyl‑2‑propyl‑1,3‑propanediol dicarbamate) |
| Assay specification | typical 98‑102 % of label claim |
| Dissolution time | typical ≥85 % dissolved in 30 min (USP) |
| Purity (impurities limit) | typical ≤0.5 % related substances |
| Tablet weight (typical) | typical 0.65 g |
| Hardness (typical) | typical 7 kp |
| Packaging | typical 100 tablets per bottle, HDPE |
| Storage condition (standard) | standard 20‑25 °C, protected from moisture |

Safe Health Mart - Buy Medicines Online is located at 6670 Villa Sonrisa Dr 222, Boca Raton, Florida, United States. The supplier is listed in the organic tier and carries a harbor trust tier, indicating a moderate level of verification on the platform. Its response metrics show a 0 % response rate and no average response time disclosed, suggesting that direct communication is required to gauge responsiveness. The company states that it sources the Carisoprodol tablets directly from licensed manufacturers.
The profile does not provide specific details on production capacity, certifications or client references, and it does not claim any awards. Safe Health Mart emphasizes compliance with FDA regulations for the active ingredient and highlights its ability to ship domestically within the United States. Prospective buyers should request copies of the DEA registration, certificate of analysis and manufacturing batch records to verify product authenticity. No additional historical or financial information is supplied in the listing.
Carisoprodol 350mg and 500mg tablets are prescription muscle relaxants used for short-term treatment of acute musculoskeletal pain conditions. These retail-ready pharmaceutical tablets are sourced from licensed manufacturers and comply with standard pharmaceutical specifications including proper assay, dissolution, and purity parameters. As a Schedule IV controlled substance subject to DEA regulation, international trade requires appropriate licensing and documentation, with pricing typically negotiated per unit volume for wholesale pharmaceutical import/export operations.
| 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 verify that they hold a valid DEA registration for Schedule IV substances and obtain a current certificate of analysis for the specific batch. Request the manufacturer’s batch number, expiry date and any stability data to ensure the product meets regulatory requirements. Confirm that the supplier can provide the required controlled‑substance shipping documentation, including a DEA Form 222 where applicable.
Logistics for this product are typically arranged under domestic Incoterms such as DAP or DDP, with the supplier offering door‑to‑door delivery across the United States. Lead times are not disclosed in the listing, so buyers should ask the supplier to confirm estimated shipping duration and any expedited options. Payment methods commonly accepted include irrevocable Letter of Credit and Telegraphic Transfer; the exact terms should be agreed in the purchase contract.
Quality assurance relies on standard pharmacopeial tests for assay, dissolution and impurity limits. Importers are advised to arrange third‑party inspection or request an on‑site audit of the manufacturing facility if additional assurance is needed. Documentation to retain includes the certificate of analysis, batch manufacturing record, DEA registration proof and any relevant stability or purity test reports.
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