NDC 67046-122 Divalproex Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67046 - Contract Pharmacy Services-pa
- 67046-122 - Divalproex Sodium
Product Characteristics
Product Packages
NDC Code 67046-122-30
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product Details
What is NDC 67046-122?
What are the uses for Divalproex Sodium?
Which are Divalproex Sodium 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 Divalproex Sodium 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:
- AMMONIA (UNII: 5138Q19F1X)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DIBUTYL SEBACATE (UNII: 4W5IH7FLNY)
- ETHYLCELLULOSE (UNII: 7Z8S9VYZ4B)
- HYPROMELLOSE (UNII: 3NXW29V3WO)
- OLEIC ACID (UNII: 2UMI9U37CP)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
What is the NDC to RxNorm Crosswalk for Divalproex Sodium?
- RxCUI: 1099569 - divalproex sodium 500 MG 24HR Extended Release Oral Tablet
- RxCUI: 1099569 - 24 HR divalproex sodium 500 MG Extended Release Oral Tablet
- RxCUI: 1099569 - divalproex sodium 500 MG 24 HR Extended Release Oral Tablet
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[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".