51079-475 : Divalproex Sodium 500 mg Delayed Release Tablet

NDC:	51079-475
Labeler:	Mylan Institutional Inc.
Product Type:	Human Prescription Drug
Drug Name:	Divalproex Sodium
Dosage Form:	Oral Tablet, Delayed Release
Application #:	ANDA090062
Rev. Date:	Oct 11, 2012

Appearance:

Markings:	M945
Shapes:	Oval
Colors:	Blue
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.

M945: (51079-475) Divalproex Sodium 500 mg Delayed Release Tablet by Mylan Institutional Inc.

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:

51079-475-08: 80 BLISTER PACK IN 1 BOX, UNIT‑DOSE (51079‑475‑08) > 1 TABLET, DELAYED RELEASE IN 1 BLISTER PACK (51079‑475‑01)

Active Ingredients:

Divalproex Sodium

Dosage Strength:

500 mg

Inactive Ingredients:

Ferrosoferric Oxide
Silicon Dioxide
Copovidone K25-31
Croscarmellose Sodium
Fd&c Blue No. 2
Fd&c Yellow No. 6
Hypromelloses
Lactose Monohydrate
Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
Cellulose, Microcrystalline
Polydextrose
Polyethylene Glycols
Polysorbate 80
Polyvinyl Alcohol
Propylene Glycol
Sodium Hydroxide
Talc
Titanium Dioxide
Triacetin
Triethyl Citrate

Pharmaceutical Classes:

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

NDC 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.