0615-1393 : Divalproex Sodium 125 mg Delayed Release Capsule

NDC:	0615-1393
Labeler:	Ncs Healthcare of Ky, Inc Dba Vangard Labs
Product Type:	Human Prescription Drug
Drug Name:	Divalproex Sodium
Dosage Form:	Oral Capsule
Application #:	ANDA078979
Rev. Date:	Jan 23, 2009

Appearance:

Markings:	THIS;END;UP;RDY;532
Shapes:	Capsule
Colors:	White
Size (mm):	19
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.

THIS END UP RDY 532: (55111-532) Divalproex Sodium 125 mg Delayed Release Capsule by Ncs Healthcare of Ky, Inc Dba Vangard Labs

The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

0615-1393-05: 15 CAPSULE IN 1 BLISTER PACK (0615‑1393‑05)
0615-1393-30: 30 BLISTER PACK IN 1 BOX, UNIT‑DOSE (0615‑1393‑30) > 5 CAPSULE IN 1 BLISTER PACK
0615-1393-31: 31 CAPSULE IN 1 BLISTER PACK (0615‑1393‑31)
0615-1393-39: 30 CAPSULE IN 1 BLISTER PACK (0615‑1393‑39)

Active Ingredients:

Divalproex Sodium

Dosage Strength:

125 mg

Inactive Ingredients:

Ferrosoferric Oxide
D&c Red No. 28
Ethylcelluloses
Fd&c Blue No. 1
Gelatin
Hypromelloses
Magnesium Stearate
Titanium Dioxide
Triethyl Citrate
Raw Sugar

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 0615-1393 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.