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Divalproex sodium - Medication Information

Product NDC Code 65841-639
Drug Name

Divalproex sodium

Type Generic
Pharm Class Anti-epileptic Agent [EPC],
Decreased Central Nervous System Disorganized Electrical Activity [PE],
Mood Stabilizer [EPC]
Active Ingredients
Divalproex sodium 125 mg/1
Route ORAL
Dosage Form CAPSULE, COATED PELLETS
RxCUI drug identifier 1099596
Application Number ANDA078919
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
65841-639-01 100 capsule, coated pellets in 1 bottle (65841-639-01)
65841-639-10 1000 capsule, coated pellets in 1 bottle (65841-639-10)
65841-639-30 10 blister pack in 1 carton (65841-639-30) / 10 capsule, coated pellets in 1 blister pack
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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