70518-1758 : Depakote 250 mg Oral Tablet, Extended Release


NDC70518-1758
Labeler: Remedyrepack Inc.
Product Type: Human Prescription Drug
Drug Name:  Depakote ER
Dosage Form: Oral Tablet, Extended Release
Application #: NDA021168
Rev. Date: 


Appearance:


Markings: a;HF
Shapes:  Oval
Colors:  White
Size (mm): 17
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.

a HF: (0074-3826) Depakote 250 mg Oral Tablet, Extended Release by Remedyrepack 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:

  • 70518-1758-0: 30 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK (70518‑1758‑0)

Active Ingredients:

  • Divalproex Sodium

Dosage Strength:

  • 250 mg

Inactive Ingredients:

  • Titanium Dioxide
  • Silicon Dioxide
  • Potassium Sorbate
  • Propylene Glycol
  • Fd&c Blue No. 1
  • Cellulose, Microcrystalline
  • Triacetin
  • Lactose, Unspecified Form
  • Hypromellose, Unspecified
  • Polyethylene Glycol, Unspecified /

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 70518-1759 Depakote 500 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 70518-3754 Depakote 250 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 24236-411 Depakote 250 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 24236-979 Depakote 500 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 0074-7401 Depakote 250 mg Oral Tablet, Extended Release by Abbvie Inc.
  • 0074-7402 Depakote 500 mg Oral Tablet, Extended Release by Abbvie Inc.
  • 43353-310 Depakote 500 mg Oral Tablet, Extended Release by Aphena Pharma Solutions - Tennessee, LLC

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 70518-1758 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.