63629-4185 : Divalproex Sodium 250 mg Delayed Release Tablet

NDC:	63629-4185
Labeler:	Bryant Ranch Prepack
Product Type:	Human Prescription Drug
Drug Name:	Divalproex Sodium Delayed-release
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA090210
Rev. Date:	Nov 30, 2009

Appearance:

Markings:	2706;V
Shapes:	Oval
Colors:	Orange
Size (mm):	14
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.

2706 V: (0603-3442) Divalproex Sodium 250 mg Delayed Release Tablet by Bryant Ranch Prepack

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:

63629-4185-1: 30 TABLET, FILM COATED IN 1 BOTTLE (63629‑4185‑1)
63629-4185-2: 60 TABLET, FILM COATED IN 1 BOTTLE (63629‑4185‑2)
63629-4185-3: 90 TABLET, FILM COATED IN 1 BOTTLE (63629‑4185‑3)
63629-4185-4: 120 TABLET, FILM COATED IN 1 BOTTLE (63629‑4185‑4)

Active Ingredients:

Divalproex Sodium

Dosage Strength:

250 mg

Inactive Ingredients:

Starch, Corn
Hypromelloses
Methacrylic Acid
Povidone
Silicon Dioxide
Sodium Bicarbonate
Sodium Lauryl Sulfate
Talc
Titanium Dioxide
Triacetin
Triethyl Citrate
Fd&c Yellow No. 6
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 63629-4185 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.