0904-6363 : Divalproex Sodium 250 mg Oral Tablet, Extended Release


NDC: 0904-6363
Labeler: Major Pharmaceuticals
Product Type: Human Prescription Drug
Drug Name:  Divalproex Sodium
Dosage Form: Oral Tablet, Extended Release
Application #: ANDA090161
Rev. Date: 


Appearance:


Markings: R;533
Shapes:  Round
Colors:  White
Size (mm): 11
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.

NDC Package Codes:

  • 0904-6363-45: 80 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK (0904‑6363‑45)
  • 0904-6363-61: 100 BLISTER PACK IN 1 CARTON (0904‑6363‑61) > 1 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK

Active Ingredients:

  • Divalproex Sodium

Dosage Strength:

  • 250 mg

Inactive Ingredients:

  • Hypromelloses
  • Hydroxyethyl Cellulose (2000 Mpa.s At 1%)
  • Lactose Monohydrate
  • Cellulose, Microcrystalline
  • Silicon Dioxide
  • Titanium Dioxide
  • Polyethylene Glycol 400

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.
  • 0904-5990 Divalproex Sodium 250 mg 24 Hr Extended Release Tablet by Major Pharmaceuticals
  • 0904-6073 Divalproex Sodium 500 mg 24 Hr Extended Release Tablet by Major Pharmaceuticals
  • 0904-6364 Divalproex Sodium 500 mg Oral Tablet, Extended Release by Major Pharmaceuticals
  • 0904-6615 Divalproex Sodium 125 mg Oral Capsule by Major Pharmaceuticals
  • 0904-6860 Divalproex Sodium 250 mg Oral Tablet, Delayed Release by Major Pharmaceuticals
  • 0904-6861 Divalproex Sodium 500 mg Oral Tablet, Delayed Release by Major Pharmaceuticals
  • 0904-7181 Divalproex Sodium 250 mg Oral Tablet, Extended Release by Major Pharmaceuticals
  • 0904-7182 Divalproex Sodium 500 mg Oral Tablet, Extended Release by Major Pharmaceuticals
  • 0074-0805 Divalproex Sodium by Abbvie Inc.
  • 0093-7439 Divalproex Sodium 125 mg Delayed Release Tablet by Teva Pharmaceuticals USA Inc
  • 0093-7440 Divalproex Sodium (Valproic Acid 250 mg) by Teva Pharmaceuticals USA Inc
  • 0093-7441 Divalproex Sodium 500 mg Delayed Release Tablet by Teva Pharmaceuticals USA Inc
  • 0115-6911 Divalproex Sodium 250 mg 24 Hr Extended Release Tablet by Global Pharmaceuticals, Division of Impax Laboratories Inc.
  • 0115-6922 Divalproex Sodium 500 mg 24 Hr Extended Release Tablet by Global Pharmaceuticals, Division of Impax Laboratories Inc.
  • 0245-0180 Divalproex Sodium 125 mg Delayed Release Tablet by Upsher-smith Laboratories, Inc.
  • 0245-0181 Divalproex Sodium 250 mg Delayed Release Tablet by Upsher-smith Laboratories, Inc.
  • 0245-0182 Divalproex Sodium 500 mg Delayed Release Tablet by Upsher-smith Laboratories, Inc.
  • 0378-0472 Divalproex Sodium 250 mg 24 Hr Extended Release Tablet by Mylan Pharmaceuticals Inc.
  • 0378-0473 Divalproex Sodium 500 mg 24 Hr Extended Release Tablet by Mylan Pharmaceuticals Inc.
  • 0378-1043 Divalproex Sodium 125 mg Delayed Release Tablet by Mylan Pharmaceutical Inc.
  • More related products ...

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.