SODIUM VALPROATE 333 VALPROIC ACID CONTROLLED RELEASE 145 TABLET
SODIUM VALPROATE 333 VALPROIC ACID CONTROLLED RELEASE 145 TABLET
SODIUM VALPROATE 333 VALPROIC ACID CONTROLLED RELEASE 145 TABLET
SODIUM VALPROATE 333 VALPROIC ACID CONTROLLED RELEASE 145 TABLET
SODIUM VALPROATE 333 VALPROIC ACID CONTROLLED RELEASE 145 TABLET
SODIUM VALPROATE 333 VALPROIC ACID CONTROLLED RELEASE 145 TABLET
SODIUM VALPROATE 333 VALPROIC ACID CONTROLLED RELEASE 145 TABLET
SODIUM VALPROATE 333 VALPROIC ACID CONTROLLED RELEASE 145 TABLET

SODIUM VALPROATE 333 VALPROIC ACID CONTROLLED RELEASE 145 TABLET

Price 55.0 INR/ Piece

MOQ : 100 Pieces

SODIUM VALPROATE 333 VALPROIC ACID CONTROLLED RELEASE 145 TABLET Specification

  • Life Span
  • 36 months (typical) from manufacturing date.
  • Origin of Medicine
  • India
  • Packaging Type
  • Blister strip
  • Salt Composition
  • Sodium Valproate 333 mg + Valproic Acid 145 mg
  • Brand Name
  • Not specified in image, typically manufacturer dependent.
  • Pacakaging (Quantity Per Box)
  • 10x10 tablets (varies depending on manufacturer).
  • Indication
  • Indicated for the treatment of epilepsy, prevention of seizures, and bipolar disorder.
  • Dosage Form
  • Controlled release tablet
  • Drug Type
  • Allopathic
  • Ingredients
  • Each tablet contains Sodium Valproate 333 mg and Valproic Acid 145 mg (controlled release).
  • Physical Form
  • Tablets
  • Function
  • Anticonvulsant, mood stabilizer.
  • Recommended For
  • Epilepsy, bipolar disorder, and other neurological conditions as prescribed by a physician.
  • Dosage
  • As directed by the physician. Typical adult dose: adjust based on clinical response.
  • Dosage Guidelines
  • Swallow whole, do not crush or chew. Take after meals to minimize gastric irritation.
  • Suitable For
  • Adults and children above 12 years, as directed by a doctor.
  • Quantity
  • Varies (commonly 10 tablets per strip/box configuration may differ per packaging).
  • Storage Instructions
  • Store in a cool, dry place away from sunlight and moisture.
  • Precautions
  • Monitor liver function, avoid abrupt discontinuation, periodically check blood counts
  • Appearance
  • White to off-white round tablets
  • Contraindications
  • Known hypersensitivity to valproate, severe liver dysfunction, urea cycle disorders
  • Side Effects
  • May include nausea, tremor, lethargy, increased liver enzymes, weight gain
  • MRP (if applicable)
  • Variable (dependent on manufacturer and region)
  • Controlled Release Mechanism
  • Extended release for sustained therapeutic levels
  • ATC Code
  • N03AG01
  • Regulatory Status
  • Approved by Drug Controller General (India)
  • Route of Administration
  • Oral
  • Prescription Status
  • Prescription only
 

SODIUM VALPROATE 333 VALPROIC ACID CONTROLLED RELEASE 145 TABLET Trade Information

  • Minimum Order Quantity
  • 100 Pieces
  • Payment Terms
  • Cash in Advance (CID)
  • Supply Ability
  • 1000 Pieces Per Month
  • Sample Available
  • No
  • Packaging Details
  • 10X10
  • Main Domestic Market
  • All India
 

About SODIUM VALPROATE 333 VALPROIC ACID CONTROLLED RELEASE 145 TABLET

Genericart Sodium Valproate+Valproic Acid 333mg/145mg Tablet CR is a combination of two medicines used to treat epilepsy, a neurological disorder in which there are recurrent episodes of seizures or fits. It controls the abnormal activity of the brain, relaxes the nerves and hence, prevents seizures or fits.

Controlled Release for Steady Therapeutic Effect

This medication utilizes an extended-release mechanism, ensuring a consistent level of active ingredients in the bloodstream over time. By releasing Sodium Valproate and Valproic Acid gradually, it reduces dosing frequency and helps maintain stable control of symptoms with minimized peaks and troughs.


Indications and Recommended Usage

SODIUM VALPROATE 333 VALPROIC ACID CONTROLLED RELEASE 145 TABLET is indicated for the treatment of epilepsy, seizure prevention, and bipolar disorder. Dosage is tailored by a physician based on each patient's clinical response. The tablets are suitable for adults and children above 12 years, and should only be taken under medical supervision.


Important Safety Precautions

Regular monitoring of liver function and blood counts is required during treatment. The medicine should not be discontinued suddenly without consulting a healthcare provider. Patients with severe liver dysfunction, urea cycle disorders, or known hypersensitivity to valproate should not use this product. Common side effects include nausea, tremor, and lethargy.

FAQ's of SODIUM VALPROATE 333 VALPROIC ACID CONTROLLED RELEASE 145 TABLET:


Q: How should SODIUM VALPROATE 333 VALPROIC ACID CONTROLLED RELEASE 145 TABLET be taken?

A: This medication should be swallowed whole, not crushed or chewed, preferably after meals to reduce gastric irritation. Always follow your physician's specific instructions for dosage and timing.

Q: What conditions are treated with this controlled release tablet?

A: It is indicated for managing epilepsy, preventing seizures, and as a mood stabilizer for bipolar disorder. The prescription must come from a healthcare professional, who will determine if it is appropriate for your condition.

Q: When should liver function and blood counts be monitored while using this medication?

A: Liver function tests and blood counts should be performed prior to starting therapy and then periodically during treatment, as recommended by your doctor, to monitor for potential side effects.

Q: Where should the tablets be stored to maintain their effectiveness?

A: Store the tablets in a cool, dry place away from sunlight and moisture. Always keep medications out of reach of children and do not use after the expiration date.

Q: What benefits does the controlled release mechanism offer?

A: The extended-release feature allows a gradual and prolonged release of medication, maintaining stable blood levels, improving symptom control, and potentially reducing side effects compared to immediate-release formulations.

Q: What are the main precautions and contraindications for this medication?

A: Major precautions include monitoring liver function and blood counts, and avoiding abrupt discontinuation. It is contraindicated in cases of known hypersensitivity to valproate, severe liver dysfunction, or urea cycle disorders.

Q: Who can use this medication and in what quantities is it typically available?

A: SODIUM VALPROATE 333 VALPROIC ACID CONTROLLED RELEASE 145 TABLET is prescribed for adults and children above 12 years, as directed by a physician. It is usually available in blister strips, typically with 10 tablets per strip, though packaging can vary by manufacturer.

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