Divalproex Sodium 81469-0492

Product NDC

81469-0492

Manufacturer: First Nation Group, Llc
Dosage Form: Capsule, Coated Pellets
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: November 10, 2025
Listing Expires: December 31, 2027
Application: ANDA217358

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Active Ingredients

Ingredient	Strength
Divalproex Sodium	125 mg/1

Drug Class

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

Packaging Options(2)

81469-0492-01

100 CAPSULE, COATED PELLETS in 1 BOTTLE (81469-492-01)

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81469-0492-10

1000 CAPSULE, COATED PELLETS in 1 BOTTLE (81469-492-10)

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