37662-2862 : Divalproex Sodium 6 [Hp_c]/1 Oral Pellet


NDC: 37662-2862
Labeler: Hahnemann Laboratories, Inc.
Product Type: Human OTC Drug
Drug Name:  Divalproex Sodium
Dosage Form: Oral Pellet
Rev. Date: 


NDC Package Codes:

  • 37662-2862-1: 200 PELLET IN 1 VIAL, GLASS (37662‑2862‑1)
  • 37662-2862-2: 1200 PELLET IN 1 BOTTLE, GLASS (37662‑2862‑2)
  • 37662-2862-3: 4000 PELLET IN 1 BOTTLE, GLASS (37662‑2862‑3)

Active Ingredients:

  • Valproate Sodium

Dosage Strength:

  • 6 [hp_C]/1

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.
  • 37662-0725 Divalproex Sodium 6 [Hp_c]/1 Oral Pellet by Hahnemann Laboratories, Inc.
  • 37662-0726 Divalproex Sodium 12 [Hp_c]/1 Oral Pellet by Hahnemann Laboratories, Inc.
  • 37662-0727 Divalproex Sodium 30 [Hp_c]/1 Oral Pellet by Hahnemann Laboratories, Inc.
  • 37662-0728 Divalproex Sodium 100 [Hp_c]/1 Oral Pellet by Hahnemann Laboratories, Inc.
  • 37662-0729 Divalproex Sodium 200 [Hp_c]/1 Oral Pellet by Hahnemann Laboratories, Inc.
  • 37662-0730 Divalproex Sodium 500 [Hp_c]/1 Oral Pellet by Hahnemann Laboratories, Inc.
  • 37662-0731 Divalproex Sodium 1 [Hp_m]/1 Oral Pellet by Hahnemann Laboratories, Inc.
  • 37662-0732 Divalproex Sodium 1 [Hp_q]/1 Oral Pellet by Hahnemann Laboratories, Inc.
  • 37662-2863 Divalproex Sodium 12 [Hp_c]/1 Oral Pellet by Hahnemann Laboratories, Inc.
  • 37662-2864 Divalproex Sodium 30 [Hp_c]/1 Oral Pellet by Hahnemann Laboratories, Inc.
  • 37662-2865 Divalproex Sodium 100 [Hp_c]/1 Oral Pellet by Hahnemann Laboratories, Inc.
  • 37662-2866 Divalproex Sodium 200 [Hp_c]/1 Oral Pellet by Hahnemann Laboratories, Inc.
  • 37662-2867 Divalproex Sodium 500 [Hp_c]/1 Oral Pellet by Hahnemann Laboratories, Inc.
  • 37662-2868 Divalproex Sodium 1 [Hp_m]/1 Oral Pellet by Hahnemann Laboratories, Inc.
  • 37662-2869 Divalproex Sodium 10 [Hp_m]/1 Oral Pellet by Hahnemann Laboratories, 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.
  • 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.