68788-7177 : Divalproex Sodium 500 mg Oral Tablet, Film Coated, Extended Release


NDC68788-7177
Labeler: Preferred Pharmaceuticals Inc.
Product Type: Human Prescription Drug
Drug Name:  Divalproex Sodium
Dosage Form: Oral Tablet, Film Coated, Extended Release
Application #: ANDA202419
Rev. Date: 


Appearance:


Markings: I50
Shapes:  Oval
Colors:  Gray
Size (mm): 19
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:

  • 68788-7177-3: 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (68788‑7177‑3)
  • 68788-7177-6: 60 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (68788‑7177‑6)
  • 68788-7177-9: 90 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (68788‑7177‑9)

Active Ingredients:

  • Divalproex Sodium

Dosage Strength:

  • 500 mg

Inactive Ingredients:

  • Fd&c Blue No. 1
  • Fd&c Blue No. 2
  • Hypromellose 2208 (100 Mpa.s)
  • Hypromellose 2910 (3 Mpa.s)
  • Hypromellose 2910 (6 Mpa.s)
  • Mannitol
  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Polyethylene Glycol 8000
  • Starch, Corn
  • Propylene Glycol
  • Shellac
  • Microcrystalline Cellulose
  • Silicon Dioxide
  • Titanium Dioxide
  • Triacetin
  • Ferrosoferric Oxide
  • Ferric Oxide Yellow
  • Polydextrose /

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.
  • 68788-7183 Divalproex Sodium 250 mg Oral Tablet, Delayed Release by Preferred Pharmaceuticals Inc.
  • 68788-7295 Divalproex Sodium 500 mg Oral Tablet, Extended Release by Preferred Pharmaceuticals Inc.
  • 68788-8145 Divalproex Sodium 250 mg Oral Tablet, Delayed Release by Preferred Pharmaceuticals Inc.
  • 68788-8085 Divalproex Sodium 500 1/1 Oral Tablet, Extended Release by Preferred Pharmaceuticals, Inc.
  • 68788-8358 Divalproex Sodium 500 mg Oral Tablet, Extended Release by Preferred Pharmaceuticals, Inc.
  • 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.
  • 0378-1044 Divalproex Sodium 250 mg Delayed Release Tablet by Mylan Pharmaceutical Inc.
  • 0378-1045 Divalproex Sodium 500 mg Delayed Release Tablet by Mylan Pharmaceutical Inc.
  • 0378-8008 Divalproex Sodium 125 mg Delayed Release Capsule by Mylan Pharmaceuticals Inc.
  • More related products ...

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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.