0615-7532 : Divalproex Sodium 250 mg Delayed Release Tablet

NDC:	0615-7532
Labeler:	Ncs Healthcare of Ky, Inc Dba Vangard Labs
Product Type:	Human Prescription Drug
Drug Name:	Divalproex Sodium
Dosage Form:	Oral Tablet, Delayed Release
Application #:	ANDA078182
Rev. Date:	Jan 21, 2011

Appearance:

Markings:	U;S;181
Shapes:	Oval
Colors:	Pink
Size (mm):	15
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.

U S 181: (0245-0181) Divalproex Sodium 250 mg Delayed Release Tablet 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:

0615-7532-30: 6 BLISTER PACK IN 1 BOX, UNIT‑DOSE (0615‑7532‑30) > 5 TABLET, DELAYED RELEASE IN 1 BLISTER PACK
0615-7532-31: 31 TABLET, DELAYED RELEASE IN 1 BLISTER PACK (0615‑7532‑31)
0615-7532-39: 30 TABLET, DELAYED RELEASE IN 1 BLISTER PACK (0615‑7532‑39)

Active Ingredients:

Divalproex Sodium

Dosage Strength:

250 mg

Inactive Ingredients:

Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
Povidones
Starch, Corn
Silicon Dioxide
Sodium Bicarbonate
Sodium Lauryl Sulfate
Talc
Triethyl Citrate
Titanium Dioxide
Vanillin
Fd&c Yellow No. 6
Ferric Oxide Red

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 0615-7532 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.