52125-134 : Divalproex Sodium 250 mg Delayed Release Tablet
| NDC: | 52125-134 |
| Labeler: | Remedyrepack Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Divalproex Sodiumdelayed-release Delayed-release |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | ANDA090210 |
| Rev. Date: |
Appearance:
| Markings: | 2706;V |
| Shapes: |
Oval |
| Colors: |
 Orange |
| Size (mm): | 14 |
| 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. | |
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:
- 52125-134-02: 30 TABLET, FILM COATED IN 1 BLISTER PACK (52125‑134‑02)
Active Ingredients:
- Divalproex Sodium
Dosage Strength:
- 250 mg
Inactive Ingredients:
- Starch, Corn
- Hypromelloses
- Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
- Povidone K12
- Silicon Dioxide
- Sodium Bicarbonate
- Sodium Lauryl Sulfate
- Talc
- Titanium Dioxide
- Triacetin
- Triethyl Citrate
- Fd&c Red No. 40
- Fd&c Yellow No. 6
- Ferric Oxide Yellow
- D&c Red No. 27
- Fd&c Blue No. 2
Pharmaceutical Classes:
- Anti-epileptic Agent [EPC]
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- Mood Stabilizer [EPC]
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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.