Divalproex Sodium 48433-0033

Product NDC

48433-0033

Manufacturer: Safecor Health, Llc
Dosage Form: Tablet, Film Coated, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: February 24, 2026
Listing Expires: December 31, 2027
Application: ANDA077567

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Active Ingredients

Ingredient	Strength
Divalproex Sodium	250 mg/1

Drug Class

Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]Mood Stabilizer [EPC]

Packaging Options(1)

48433-0033-08

80 BLISTER PACK in 1 CARTON (48433-033-08) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (48433-033-01)

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