0615-8330 : Divalproex Sodium 500 mg Oral Tablet, Extended Release

NDC:	0615-8330
Labeler:	Ncs Healthcare of Ky, Inc Dba Vangard Labs
Product Type:	Human Prescription Drug
Drug Name:	Divalproex Sodium
Dosage Form:	Oral Tablet, Extended Release
Application #:	ANDA090070
Rev. Date:	Aug 11, 2013

Appearance:

Markings:	R;534
Shapes:	Oval
Colors:	Gray
Size (mm):	20
Segments: ^*	1
^* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

0615-8330-30: 6 BLISTER PACK IN 1 BOX, UNIT‑DOSE (0615‑8330‑30) > 5 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK
0615-8330-39: 30 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK (0615‑8330‑39)

Active Ingredients:

Divalproex Sodium

Dosage Strength:

500 mg

Inactive Ingredients:

Hypromellose 2208 (15000 Mpa.s)
Hydroxyethyl Cellulose (2000 Cps At 1%)
Lactose Monohydrate
Cellulose, Microcrystalline
Silicon Dioxide
Hydroxypropyl Cellulose (1600000 Wamw)
Titanium Dioxide
Ferrosoferric Oxide
Ferric Oxide Yellow /

Pharmaceutical Classes:

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

NDC QR Code

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NDC 0615-8330 QR Code

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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.