Harmful if swallowed
This substance is a potent pharmaceutical agent. Avoid contact with skin, eyes, and respiratory tract. Use appropriate personal protective equipment during handling.
Eyes: Flush with plenty of water for 15 minutes and seek medical attention.
Skin: Wash with soap and water; remove contaminated clothing.
Atomoxetine Hydrochloride is a white to off-white crystalline powder that serves as a critical pharmaceutical ingredient. It is chemically identified as (–)-N-methyl-3-phenyl-3-(o-tolyloxy)propylamine hydrochloride, widely recognized for its efficacy in treating ADHD in both pediatric and adult populations.
In the Indian pharmaceutical landscape, this chemical is manufactured by specialized API facilities catering to both domestic generic drug manufacturers and international export markets. It is subject to stringent regulatory oversight by the CDSCO and must comply with pharmacopeial standards such as USP or BP to ensure therapeutic safety and efficacy.
Procurement of Atomoxetine Hydrochloride requires rigorous verification of the supplier's GMP certification and the availability of a Certificate of Analysis (CoA). Buyers should prioritize vendors who provide comprehensive documentation, including impurity profiles and stability data, to facilitate smooth regulatory filings and quality assurance.
Atomoxetine Hydrochloride 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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Atomoxetine Hydrochloride 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, our suppliers provide GMP-certified Atomoxetine Hydrochloride with full documentation.
Standard pharmaceutical grade is ≥ 98.0%, while analytical standards are ≥ 99.5%.
Yes, every batch is supplied with a comprehensive CoA including impurity profiles.
Yes, it is a pharmaceutical ingredient subject to CDSCO guidelines and standard drug manufacturing regulations.
Lead times typically range from 2 to 4 weeks depending on batch availability and testing requirements.
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