Sodium Valproate
Generic Name: sodium valproate
Dosage form: POWDER. Active ingredients: VALPROATE SODIUM (25 kg/25kg). Category: BULK INGREDIENT.
Overview
Dosage form: POWDER. Active ingredients: VALPROATE SODIUM (25 kg/25kg). Category: BULK INGREDIENT.
Dosage
Available as powder.
Related Medications
Thyroidinum, Baryta Carb., Berber. Vulg., Bryonia, Calc. Carb., Cinchona, Conium, Digitalis, Ferrum Picricum, Hydrastis, Iodium, Lycopodium, Nux Vom., Pareira, Pulsatilla, Sabal, Selenium, Staphysag., Thuja Occ.,trifolium Pratense, Echinacea, Lappa, Solidago
thyroidinum, baryta carb., berber. vulg., bryonia, calc. carb., cinchona, conium, digitalis, ferrum picricum, hydrastis, iodium, lycopodium, nux vom., pareira, pulsatilla, sabal, selenium, staphysag., thuja occ.,trifolium pratense, echinacea, lappa, solidago
Non-Standardized Plant Allergenic Extract [EPC]
OTC - PURPOSE SECTION Formulated for associated symptoms such as discomfort, or frequent, incomplete or difficult urination.
Thrombin Topical Recombinant
thrombin topical recombinant
11 DESCRIPTION RECOTHROM Thrombin topical (Recombinant), is a human coagulation protein produced via recombinant DNA technology from a genetically modified CHO cell line. RECOTHROM is identical in amino acid sequence and structurally similar to naturally occurring human thrombin.
Potassium Phosphates In Sodium Chloride
potassium phosphates in sodium chloride
11 DESCRIPTION Potassium Phosphates in 0.9% Sodium Chloride Injection, for intravenous use, is a phosphorus replacement product containing phosphorus 0.06 mmol/mL and potassium 0.088 mEq/mL. It is a sterile, non-pyrogenic, ready-to-use diluted solution containing a mixture of monobasic potassium phosphate, USP and dibasic potassium phosphate, USP in 0.9% sodium chloride. No dilution is required before administration. It is supplied in 250 mL single-dose intravenous infusion bag.
Medical Disclaimer
This drug information is for educational purposes only and should not replace professional medical advice. Drug information is sourced from the FDA National Drug Code Directory and Structured Product Labeling. Always consult with a healthcare provider before starting, stopping, or changing any medication.