About OXETACAINE IP
Oxetacaine, as per the Indian Pharmacopoeia (IP), is a pharmaceutical compound renowned for its dual therapeutic roles as a local anesthetic and antacid. It is widely used to alleviate pain and discomfort associated with gastrointestinal conditions such as gastritis, esophagitis, and peptic ulcers.
The IP outlines stringent standards to ensure the quality, efficacy, and safety of Oxetacaine for medicinal applications.
High-Quality Pharmaceutical IngredientOxetacaine IP is a premium active pharmaceutical ingredient (API) produced in India, recognized for its purity (99%) and compliance with international pharmacopeial standards. Suitable for the treatment of gastritis and peptic ulcers, it is trusted by manufacturers for its quality, safety, and consistent performance, thanks to rigorous WHO-GMP certified processes.
Versatile Applications in FormulationsIdeal for syrups, gels, and oral suspensions, Oxetacaine IP offers significant versatility to pharmaceutical manufacturers. Its efficacy as a local anesthetic brings rapid pain relief for gastrointestinal ailments, making it a preferred choice for antacid and digestive remedies.
Safe, Stable, and Reliable SupplyPackaged in HDPE drums or custom containers, Oxetacaine IP ensures product integrity with a shelf life of 36 months. It is non-hazardous under transportation regulations, with each batch tested for microbial safety and impurity levels as per pharmacopeial requirements. Proper storage in cool, dry conditions is recommended.
FAQ's of OXETACAINE IP:
Q: How is Oxetacaine IP typically used in pharmaceutical manufacturing?
A: Oxetacaine IP serves as a local anesthetic in the preparation of syrups, gels, and oral suspensions, primarily for the relief of pain and discomfort associated with gastritis and peptic ulcers. It is exclusively used in formulating pharmaceutical products and not intended for household use.
Q: What benefits does Oxetacaine IP offer to manufacturers?
A: With a purity not less than 99% and compliance with pharmacopeial standards for impurities and microbial limits, Oxetacaine IP ensures reliable efficacy and quality in finished products. Its safety profile and high stability provide added value during the product development process.
Q: When should Oxetacaine IP be stored, and how long is its shelf life?
A: Oxetacaine IP should be stored in tightly closed containers, kept in a cool, dry place to maintain product quality. With proper storage, the shelf life extends up to 36 months from the date of manufacture.
Q: Where is Oxetacaine IP manufactured and exported from?
A: Oxetacaine IP is manufactured in a WHO-GMP certified facility in India and is exported globally, with packaging options customizable according to client requirements.
Q: What process ensures the safety and quality of Oxetacaine IP?
A: Each batch of Oxetacaine IP undergoes stringent quality control, including identification testing according to IP specifications, impurity profiling, and microbial testing, all adhering to pharmacopeial requirements. The product is manufactured under strict WHO-GMP standards.
Q: How should Oxetacaine IP be transported and what are its packaging options?
A: Oxetacaine IP is classified as non-hazardous for transportation. It is available in HDPE drums or custom pack sizes to fit diverse manufacturing needs and ensure safe delivery.
Q: What are the key physicochemical properties of Oxetacaine IP?
A: Oxetacaine IP appears as a white to off-white, odorless crystalline powder with a melting point of 121-123C. It is slightly soluble in water but freely soluble in ethanol, with a molecular weight of 309.4 g/mol and meets stringent limits for moisture, heavy metals, and residue on ignition.