Divalproex Sodium 60687-0915

Product NDC

60687-0915

Manufacturer: American Health Packaging
Dosage Form: Tablet, Film Coated, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: December 29, 2025
Listing Expires: December 31, 2027
Application: ANDA214643

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Active Ingredients

Ingredient	Strength
Divalproex Sodium	500 mg/1

Drug Class

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

Packaging Options(2)

60687-0915-01

100 BLISTER PACK in 1 CARTON (60687-915-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-915-11)

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60687-0915-02

80 BLISTER PACK in 1 CARTON (60687-915-02) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-915-93)

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