50090-5842 : Divalproex Sodium 500 mg Oral Tablet, Delayed Release

NDC:	50090-5842
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Divalproex Sodium
Dosage Form:	Oral Tablet, Delayed Release
Application #:	ANDA090554
Rev. Date:	Oct 24, 2014

NDC Package Codes:

50090-5842-0: 90 TABLET, DELAYED RELEASE IN 1 BOTTLE (50090‑5842‑0)

Active Ingredients:

Divalproex Sodium

Dosage Strength:

500 mg

Pharmaceutical Classes:

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

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.