0245-0182 : Divalproex Sodium 500 mg Delayed Release Tablet


NDC: 0245-0182
Labeler: Upsher-smith Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name:  Divalproex Sodium
Dosage Form: Oral Tablet, Delayed Release
Application #: ANDA078182
Rev. Date: 


Appearance:


Markings: U;S;182
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.

U S 182: (0245-0182) Divalproex Sodium 500 mg Delayed Release Tablet by Upsher-smith Laboratories, 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:

  • 0245-0182-01: 10 BLISTER PACK IN 1 CARTON (0245‑0182‑01) > 10 TABLET, DELAYED RELEASE IN 1 BLISTER PACK (0245‑0182‑89)
  • 0245-0182-11: 100 TABLET, DELAYED RELEASE IN 1 BOTTLE (0245‑0182‑11)
  • 0245-0182-15: 500 TABLET, DELAYED RELEASE IN 1 BOTTLE (0245‑0182‑15)

Active Ingredients:

  • Divalproex Sodium

Dosage Strength:

  • 500 mg

Inactive Ingredients:

  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Povidones
  • Starch, Corn
  • Silicon Dioxide
  • Sodium Bicarbonate
  • Sodium Lauryl Sulfate
  • Talc
  • Triethyl Citrate
  • Titanium Dioxide
  • Vanillin
  • Fd&c Red No. 40

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.
  • 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.
  • 0832-7122 Divalproex Sodium 125 mg Oral Tablet, Delayed Release by Upsher-smith Laboratories, Inc.
  • 0832-7123 Divalproex Sodium 250 mg Oral Tablet, Delayed Release by Upsher-smith Laboratories, Inc.
  • 0832-7124 Divalproex Sodium 500 mg Oral Tablet, Delayed Release by Upsher-smith 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.
  • 0115-6922 Divalproex Sodium 500 mg 24 Hr Extended Release Tablet by Global Pharmaceuticals, Division of Impax 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
  • More related products ...

NDC QR Code

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NDC 0245-0182 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.