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| Product NDC Code | 65841-639 | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| Drug Name | Divalproex sodium |
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| Type | Generic | ||||||||
| Pharm Class | Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC] |
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| Active Ingredients |
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| Route | ORAL | ||||||||
| Dosage Form | CAPSULE, COATED PELLETS | ||||||||
| RxCUI drug identifier | 1099596 | ||||||||
| Application Number | ANDA078919 | ||||||||
| Labeler Name | Zydus Lifesciences Limited | ||||||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Spl product data elements
Usually a list of ingredients in a drug product.divalproex sodium divalproex sodium DIVALPROEX SODIUM VALPROIC ACID ALCOHOL AMMONIA BUTYL ALCOHOL CELLULOSE, MICROCRYSTALLINE FD&C BLUE NO. 1 FERROSOFERRIC OXIDE GELATIN HYPROMELLOSES ISOPROPYL ALCOHOL METHACRYLIC ACID POTASSIUM HYDROXIDE PROPYLENE GLYCOL SHELLAC SILICON DIOXIDE SODIUM LAURYL SULFATE TALC TITANIUM DIOXIDE TRIETHYL CITRATE WATER BLUE WHITE CAPSULE ZA66;125mg
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 65841-639-01 in bottle of 100 Capsules Divalproex sodium delayed-release capsules, USP (sprinkle) Rx only 100 capsules Divalproex Sodium Capsules Sprinkle, 125 mg
Spl medguide
Information about the patient medication guide that accompanies the drug product. Certain drugs must be dispensed with an accompanying medication guide. This field may contain information about when to consult the medication guide and the contents of the medication guide.SPL MEDGUIDE
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API