Divalproex Sodium 68084-0313

Product NDC

68084-0313

Manufacturer: American Health Packaging
Dosage Form: Capsule, Coated Pellets
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: March 18, 2009
Listing Expires: December 31, 2026
Application: ANDA078919

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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)

68084-0313-01

100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-313-01) / 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68084-313-11)

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68084-0313-65

50 BLISTER PACK in 1 CARTON (68084-313-65) / 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68084-313-11)

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