0093-7441 : Divalproex Sodium 500 mg Delayed Release Tablet


NDC: 0093-7441
Labeler: Teva Pharmaceuticals USA Inc
Product Type: Human Prescription Drug
Drug Name:  Divalproex Sodium
Dosage Form: Oral Tablet, Delayed Release
Application #: ANDA076941
Rev. Date: 


Appearance:


Markings: 93;7441
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.

93 7441: (0093-7441) Divalproex Sodium 500 mg Delayed Release Tablet by Teva Pharmaceuticals USA 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:

  • 0093-7441-01: 100 TABLET, DELAYED RELEASE IN 1 BOTTLE (0093‑7441‑01)
  • 0093-7441-05: 500 TABLET, DELAYED RELEASE IN 1 BOTTLE (0093‑7441‑05)

Active Ingredients:

  • Divalproex Sodium

Dosage Strength:

  • 500 mg

Inactive Ingredients:

  • Ammonia
  • Crospovidone
  • Hypromellose 2910 (6 Mpa.s)
  • Hypromellose Phthalate (31% Phthalate, 40 Cst)
  • Ferrosoferric Oxide
  • Lactose Monohydrate
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Polyethylene Glycol 3350
  • Polyvinyl Alcohol
  • Povidone K30
  • Starch, Corn
  • Propylene Glycol
  • Shellac
  • Silicon Dioxide
  • Talc
  • Titanium Dioxide
  • Triethyl Citrate
  • Ferric Oxide Red
  • Ferric Oxide Yellow
  • Triacetin

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.
  • 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
  • 0074-0805 Divalproex Sodium by Abbvie 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.
  • 0603-3441 Divalproex Sodium 125 mg Delayed Release Tablet by Qualitest Pharmaceuticals
  • 0603-3442 Divalproex Sodium 250 mg Delayed Release Tablet by Qualitest Pharmaceuticals
  • 0603-3443 Divalproex Sodium 500 mg Delayed Release Tablet by Qualitest Pharmaceuticals
  • 0615-1393 Divalproex Sodium 125 mg Delayed Release Capsule by Ncs Healthcare of Ky, Inc Dba Vangard Labs
  • 0615-7531 Divalproex Sodium 125 mg Delayed Release Tablet by Ncs Healthcare of Ky, Inc Dba Vangard Labs
  • 0615-7532 Divalproex Sodium 250 mg Delayed Release Tablet by Ncs Healthcare of Ky, Inc Dba Vangard Labs
  • 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.