NDC 65862-594 – Divalproex sodium

Divalproex Sodium 250 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC65862-594

Product details

Brand name
Divalproex sodium
Generic name
Divalproex sodium
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA202419
Marketed since
June 2, 2014
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent; Mood Stabilizer

Active ingredients

Uses, dosage, side effects and warnings for Divalproex Sodium →

Package NDC codes (5)

Package NDCDescriptionSince
65862-594-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-01)Jun 2, 2014
65862-594-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-05)Jun 2, 2014
65862-594-1010 BLISTER PACK in 1 CARTON (65862-594-10) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKJun 2, 2014
65862-594-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-60)Jun 2, 2014
65862-594-991000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-99)Jun 2, 2014

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