NDC 64679-974 Divalproex Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64679 - Wockhardt Usa Llc.
- 64679-974 - Divalproex Sodium
Product Characteristics
OVAL (C48345)
16 MM
W974
Product Packages
NDC Code 64679-974-01
Package Description: 100 TABLET, DELAYED RELEASE in 1 BOTTLE
NDC Code 64679-974-02
Package Description: 500 TABLET, DELAYED RELEASE in 1 BOTTLE
NDC Code 64679-974-03
Package Description: 30 TABLET, DELAYED RELEASE in 1 BOTTLE
NDC Code 64679-974-04
Package Description: 10 BLISTER PACK in 1 CARTON / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product Details
What is NDC 64679-974?
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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERYL BEHENATE/EICOSADIOATE (UNII: 73CJJ317SR)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- POVIDONE (UNII: FZ989GH94E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- STARCH, CORN (UNII: O8232NY3SJ)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
What is the NDC to RxNorm Crosswalk for Divalproex Sodium?
- RxCUI: 1099625 - divalproex sodium 125 MG Delayed Release Oral Tablet
- RxCUI: 1099678 - divalproex sodium 250 MG Delayed Release Oral Tablet
- RxCUI: 1099870 - divalproex sodium 500 MG Delayed Release Oral Tablet
* 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".