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Levocetirizine Dihydrochloride Tablets USP 10 mg
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Product is not available
Country of origin : India
Active Strength & Pharmacopoeial Grade
Levocetirizine Dihydrochloride Tablets USP 10 mg are presented as oral antihistamine tablets containing the stated strength of levocetirizine dihydrochloride. The USP designation indicates intended alignment with applicable United States Pharmacopeia requirements. Because commonly authorized levocetirizine tablet products are documented at 5 mg, buyers should specifically verify the stated 10 mg strength through the manufacturing license, finished-product specification, batch certificate of analysis (COA) and destination-market authorization.
Composition & Product Characteristics
The stated formulation contains levocetirizine dihydrochloride together with product-specific excipients required for tablet manufacture, stability and performance. Technical procurement should assess active-ingredient identity and assay, related substances, dissolution, disintegration, uniformity of dosage units, microbial quality and packaging integrity. Tablet appearance, coating, scoring, excipient composition, storage conditions and pack configuration should be confirmed from the manufacturer’s approved dossier and batch documentation.
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Additional Information
Formulation Application & Compatibility
This product is part of our Pharmaceutical Products range for pharmaceutical distributors, wholesalers and institutional procurement teams. Levocetirizine dihydrochloride is a histamine H1-receptor antagonist used in authorized antihistamine products for approved allergy-related indications. Buyers evaluating the stated 10 mg tablet must confirm that its strength, dosage form, USP specification, excipient profile, packaging and labelling are covered by the manufacturer’s license and accepted in the destination market. The medicine must be supplied and used according to its approved labelling and qualified healthcare guidance.
- Country of Origin: Confirm from the manufacturer or supplier
- Regulatory/Pharmacopoeial Compliance: Stated as USP grade; the 10 mg strength and finished-product authorization require documentary verification
- Quality Assurance / Shelf Life: Confirm batch-release testing, approved storage conditions and labelled shelf life from the COA and manufacturer documentation
Manufacturing Compliance & Documentation
Request a Levocetirizine Dihydrochloride Tablets USP 10 mg Procurement Quote
Frequently Asked Questions
- Is the 10 mg strength of Levocetirizine Dihydrochloride Tablets USP verified? Commonly referenced authorized tablets contain 5 mg. Buyers should verify the stated 10 mg strength using the manufacturing license, product-registration certificate, finished-product specification and batch COA before procurement.
- What are the minimum order quantities and bulk order options? Minimum quantities depend on the manufacturer, authorized pack configuration, destination market and regulatory requirements. Share the required volume and pack size to confirm available options.
- Are COA and USP-related documents available for this product? Documentation availability must be confirmed before ordering. Buyers should request the batch COA, USP-aligned specification, manufacturing authorization, stability information and market-registration documents.
- What logistics and lead-time considerations apply to shipments? Lead time depends on manufacturing availability, batch-release testing, packaging, documentation and import procedures. Storage and transportation must follow the manufacturer’s approved product information.
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