Sodium Bicarbonate, Citric Acid, And Anhydrous Sodium Carbonate Sachet Suppliers & Bulk Manufacturers
Available Forms: Powder
Available Strengths: Typical effervescent granules/tablets containing 324 mg sodium bicarbonate, 191 mg citric acid, and 1000 mg anhydrous sodium carbonate
Reference Brands: Alka-Seltzer, Eno
Category: OTC
Sodium Bicarbonate, Citric Acid, and Anhydrous Sodium Carbonate sachet is available in Powder and strengths such as Typical effervescent granules/tablets containing 324 mg sodium bicarbonate, 191 mg citric acid, and 1000 mg anhydrous sodium carbonate. Sourced from GMP-certified and ISO-compliant manufacturers, this API meets global pharmacopeia standards (USP/EP/JP as applicable). Ideal for pharmaceutical formulation and commercial manufacturing, Sodium Bicarbonate, Citric Acid, and Anhydrous Sodium Carbonate sachet is supplied in bulk quantities with complete regulatory support including DMF, COA, and MSDS.
| Technical Specifications & Supply Details | |
|---|---|
| Lead Time | 7 to 60 days (depending on batch size & schedule) |
| MOQ | As per manufacturer’s batch size |
| COA | Available with every batch |
| Regulatory Dossier / DMF | Available upon request |
| Export Documentation | FSC, COA, Manufacturing License, Product Permission |
| Standards | IP, BP, USP |
| Certifications | WHO-GMP, EU-GMP, USFDA (as applicable) |
Sodium Bicarbonate, Citric Acid, and Anhydrous Sodium Carbonate sachet can be exported to over 30 countries across Asia, Africa, Europe, and Latin America. Flexible packaging, competitive pricing, and a verified supplier network make Pharmatradz a trusted sourcing partner for pharmaceutical companies and contract manufacturers worldwide.
The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
Product Description:
Sodium bicarbonate, citric acid, and anhydrous sodium carbonate in the EU and US are regulated to ensure safety, efficacy, and manufacturing quality. In the US, FDA approval involves validation, safety testing, and GMP compliance, primarily for medical and industrial uses. In the EU, CE marking certifies conformity with MDR standards. These products undergo validation, stability testing, and audits, supported by comprehensive documentation including safety profiles, validation reports, and manufacturing practices. For licensing procedures, approved dossiers, and latest regulatory updates, visit Pharmatradz. Ensuring compliance guarantees access to safe, effective formulations for pharmaceutical, food, and industrial applications worldwide, supporting pH regulation, alkalinization, and effervescent product safety.
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