NDC 21695-163 Depakote
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
GRAY (C48324)
19 MM
HC
Code Structure Chart
Product Details
What is NDC 21695-163?
What are the uses for Depakote?
Which are Depakote UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIVALPROEX SODIUM (UNII: 644VL95AO6)
- VALPROIC ACID (UNII: 614OI1Z5WI) (Active Moiety)
Which are Depakote Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- LACTOSE (UNII: J2B2A4N98G)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
What is the NDC to RxNorm Crosswalk for Depakote?
- RxCUI: 1099563 - divalproex sodium 250 MG 24HR Extended Release Oral Tablet
- RxCUI: 1099563 - 24 HR divalproex sodium 250 MG Extended Release Oral Tablet
- RxCUI: 1099563 - divalproex sodium 250 MG 24 HR Extended Release Oral Tablet
- RxCUI: 1099565 - Depakote ER 250 MG 24HR Extended Release Oral Tablet
- RxCUI: 1099565 - 24 HR divalproex sodium 250 MG Extended Release Oral Tablet [Depakote]
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".