Pill Identifier Divalproex Sodium Delayed Release (sprinkle) - NDC 0781-2243
Product Code 0781-2243
Divalproex Sodium Delayed Release (sprinkle) by Sandoz Inc. is a white and blue capsule about 17 mm in size, imprinted with this;end;up;depakote;sprinkle;125;mg. The product is a with active ingredient(s) .
Divalproex Sodium Delayed Release (sprinkle)
Active Ingredient(s):
Inactive Ingredient(s):
- SILICON DIOXIDE
- TRIETHYL CITRATE
- MAGNESIUM STEARATE
- D&C RED NO. 28
- FD&C BLUE NO. 1
- FERRIC OXIDE RED
- TITANIUM DIOXIDE
- GELATIN, UNSPECIFIED
Sandoz Inc.
Product Type:
Dosage Form:
Imprint: THIS;END;UP;DEPAKOTE;SPRINKLE;125;mg What is the Imprint?
The imprint is a characteristic of an oral solid dosage form of a medicinal product, specifying the alphanumeric text that appears on the solid dosage form, including text that is embossed, debossed, engraved or printed with ink. A semicolon is used to show separation between words or line divisions.
- White (C48325)
- Blue (C48333)
Product Packages
| NDC Package Code | Package Description |
|---|---|
| 0781-2243-01 | 100 CAPSULE in 1 BOTTLE |
* Please review the disclaimer below.
Pill Identification data last updated on: December, 2018
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product. If this is an emergency, call 911 or the national Poison Help hotline at 1-800-222-1222. Most images are not part of the product labels and have not been verified by the labeler company. ALWAYS consult your physician or pharmacist with any medication-related questions.