Controlled release formulations of sodium valproate and valproic acid 300mg

Controlled release formulations of sodium valproate and valproic acid
VALPOTREAT CR  are designed to release the medication slowly and steadily over an extended period of time. VALPOTREAT CR  allows for a more consistent blood concentration of the drug, reducing the need for frequent dosing and potentially minimizing side effects.
Sodium valproate and valproic acid are anticonvulsant medications commonly used to treat epilepsy, bipolar disorder, and migraine headaches. They work by increasing the levels of a neurotransmitter called gamma-aminobutyric acid (GABA) in the brain, which helps to prevent seizures and stabilize mood.
The controlled release formulations of sodium valproate and valproic acid are typically available in the form of extended-release tablets or capsules. These formulations are designed to gradually release the medication into the body, providing a sustained therapeutic effect over a longer duration compared to immediate-release formulations.
VALPOTREAT CR  exact mechanism of controlled release can vary depending on the specific formulation and manufacturer. However, common methods include the use of specialized coatings or matrix systems that regulate the release of the medication from the tablet or capsule.
The specific dosage and administration instructions for VALPOTREAT CR  should be determined by a healthcare professional based on individual needs and medical condition. It is important to follow the prescribed dosage and schedule provided by your healthcare provider and not alter the medication regimen without their guidance.
It's worth noting that different formulations and brands of VALPOTREAT CR may have slight variations in their release profiles and effectiveness. Therefore, it is generally recommended to stick to a specific brand or formulation to ensure consistent therapy.
VALPOTREAT CR  is available in strengths of 200 , 300 and 500mg.
steris pharma deals in Generic medicines are medications that are produced and marketed after the expiration of the patent protection of the brand-name (originator) drug. Generic drugs contain the same active ingredients as the brand-name drugs and are designed to have the same dosage form, strength, route of administration, and therapeutic effect. They undergo rigorous testing to ensure they are bioequivalent to the brand-name drug, meaning they are absorbed and distributed in the body at a similar rate and to a similar extent.
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