63629-4278 : Divalproex Sodium 500 mg Delayed Release Tablet


NDC: 63629-4278
Labeler: Bryant Ranch Prepack
Product Type: Human Prescription Drug
Drug Name:  Divalproex Sodium
Dosage Form: Oral Tablet, Delayed Release
Application #: ANDA078790
Rev. Date: 


Appearance:


Markings: L007
Shapes:  Oval
Colors:  Pink
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:

  • 63629-4278-1: 60 TABLET, DELAYED RELEASE IN 1 BOTTLE (63629‑4278‑1)
  • 63629-4278-2: 30 TABLET, DELAYED RELEASE IN 1 BOTTLE (63629‑4278‑2)
  • 63629-4278-3: 90 TABLET, DELAYED RELEASE IN 1 BOTTLE (63629‑4278‑3)
  • 63629-4278-4: 180 TABLET, DELAYED RELEASE IN 1 BOTTLE (63629‑4278‑4)
  • 63629-4278-5: 120 TABLET, DELAYED RELEASE IN 1 BOTTLE (63629‑4278‑5)

Active Ingredients:

  • Divalproex Sodium

Dosage Strength:

  • 500 mg

Inactive Ingredients:

  • Cellulose, Microcrystalline
  • Silicon Dioxide
  • D&c Red No. 30
  • Fd&c Blue No. 2
  • Ferric Oxide Red
  • Hydroxypropyl Cellulose
  • Hydroxypropyl Cellulose, Low Substituted
  • Hypromellose Phthalate (24% Phthalate, 55 Cst)
  • Hypromelloses
  • Magnesium Stearate
  • Propylene Glycol
  • Shellac
  • Starch, Corn
  • Talc
  • Titanium Dioxide
  • Triethyl Citrate

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.
  • 63629-4185 Divalproex Sodium 250 mg Delayed Release Tablet by Bryant Ranch Prepack
  • 63629-4698 Divalproex Sodium 500 mg 24 Hr Extended Release Tablet by Bryant Ranch Prepack
  • 63629-7091 Divalproex Sodium 250 mg Oral Tablet, Film Coated, Extended Release by Bryant Ranch Prepack
  • 71335-0008 Divalproex Sodium 250 mg Oral Tablet, Delayed Release by Bryant Ranch Prepack
  • 71335-1883 Divalproex Sodium 500 mg Oral Tablet, Extended Release by Bryant Ranch Prepack
  • 71335-2124 Divalproex Sodium 500 mg Oral Tablet, Delayed Release by Bryant Ranch Prepack
  • 71335-2158 Divalproex Sodium 500 mg Oral Tablet, Delayed Release by Bryant Ranch Prepack
  • 71335-2277 Divalproex Sodium 250 mg Oral Tablet, Delayed Release by Bryant Ranch Prepack
  • 71335-2344 Divalproex Sodium 500 mg Oral Tablet, Delayed Release by Bryant Ranch Prepack
  • 72162-2316 Divalproex Sodium 250 mg Oral Tablet, Delayed Release by Bryant Ranch Prepack
  • 72162-2371 Divalproex Sodium 500 mg Oral Tablet, Extended Release by Bryant Ranch Prepack
  • 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.
  • 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.