Controlled Substance
This substance is a controlled drug under the NDPS Act. Handle with extreme caution; avoid inhalation, ingestion, or skin contact.
Eyes: Flush with water for 15 minutes and seek medical attention.
Skin: Wash thoroughly with soap and water; remove contaminated clothing.
Diazepam (CAS 439-14-5) is a white to off-white crystalline powder belonging to the benzodiazepine class. It acts by enhancing the effect of the neurotransmitter GABA in the brain, making it a cornerstone in the treatment of anxiety disorders, muscle spasms, and seizure conditions.
In the Indian pharmaceutical landscape, Diazepam is manufactured under strict regulatory oversight by the CDSCO and state drug control departments. It is primarily utilized by large-scale API manufacturers and pharmaceutical formulation units to produce tablets, injections, and rectal gels for both domestic consumption and international export.
Procurement of Diazepam in India requires valid Narcotic and Psychotropic Substances (NDPS) licenses. Buyers must ensure that their suppliers are GMP-certified and provide comprehensive documentation, including Certificate of Analysis (CoA) and Drug Master Files (DMF), to ensure compliance with pharmacopeial standards like USP, BP, or IP.
Diazepam pricing in India depends on grade, order quantity, and delivery location, and it moves with market conditions — so a single fixed price is rarely accurate for a specific requirement.
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Diazepam prices in India vary by grade, order quantity and delivery location, and move with market conditions. To get the current price for your requirement, submit an enquiry on Chemical Dekho and receive verified quotes from suppliers and manufacturers within 24 hours.
Yes, as it is a controlled substance under the NDPS Act, a valid license is mandatory for procurement.
We offer grades compliant with USP, BP, and IP standards.
Shipping is handled via specialized logistics providers with secure, tracked, and temperature-controlled transport.
Yes, a Drug Master File (DMF) is available upon request for qualified pharmaceutical manufacturers.
Lead time depends on regulatory documentation verification, typically 2-4 weeks.
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