50090-3616 : Divalproex Sodium 250 mg Oral Tablet, Delayed Release

NDC:	50090-3616
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Divalproex Sodium
Dosage Form:	Oral Tablet, Delayed Release
Application #:	ANDA090554
Rev. Date:	Apr 21, 2011

Appearance:

Markings:	D;85
Shapes:	Oval
Colors:	Orange
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.

D 85: (68084-776) Divalproex Sodium 250 mg Oral Tablet, Delayed Release by A-s Medication Solutions

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:

50090-3616-0: 30 TABLET, DELAYED RELEASE IN 1 BOTTLE (50090‑3616‑0)

Active Ingredients:

Divalproex Sodium

Dosage Strength:

250 mg

Inactive Ingredients:

Silicon Dioxide
Microcrystalline Cellulose
Croscarmellose Sodium
Povidone K30
Low-substituted Hydroxypropyl Cellulose, Unspecified
Talc
Methylene Chloride
Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
Diethyl Phthalate
Hypromellose 2910 (15 Mpa.s)
Triacetin
Polyvinyl Alcohol, Unspecified
Titanium Dioxide
Polyethylene Glycol 3350
Lecithin, Soybean
Vanillin
Fd&c Yellow No. 6
Ferric Oxide Yellow
Shellac
Isopropyl Alcohol
Ferrosoferric Oxide
Butyl Alcohol
Propylene Glycol
Ammonia /

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 50090-3616 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.