Chemistry Click the arrow to open the dropdown Click the button for full data set Click the button for full data set API SUPPLIERS USDMF CEP/COS JDMF EU WC KDMF NDC API Listed Suppliers API Reference Price Drugs in Development INTERMEDIATES SUPPLIERS ...
The "substitution" refers to the carbon with the leaving group attached to it. In this case the net change at that carbon is that the chloride is substituted for an oxygen in the product. In an elimination reaction, however, the chloride would just be gone with nothing taking its place (...
Chemistry Click the arrow to open the dropdown Click the button for full data set Click the button for full data set API SUPPLIERS USDMF JDMF Listed Suppliers Drugs in Development FDF Dossiers Europe Listed Dossiers Digital Content NEWS #PharmaBuzz ...
A new metal鈥搊rganic architectures, [Cu 3 (NA) 6 (DMF) 3 ] n ( 1 ), where NA stands for nicotinic acid, has been successfully synthesized and characterized by elemental analysis, IR, TG analysis and single crystal X-ray diffraction. Single-crystal X-ray diffraction reveals that the ...
Pseudoephedrine Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility. GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. ...
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP whi...
FOSETYL AL Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility. GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality s...
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP whi...
List of Drug Master Files (DMF) for 3753 Active Pharmaceutical Ingredient (API) submitted to the U.S. FDA. Original Data : FDA Website
- Cold Chemistry: D, 13C, 15N, 18O - Complex APIs - Controlled Substance - Crystallization Process - Custom Synthesis - Distillation / Liquid APIs - Fine Chemical / Intermediate - Halogenation - High Potency APIs (HPAPIs) - High Pressure Reactions (> 100 psi) - Hydrogenation - Impurity /...