NDC 16590-648 Divalproex Sodium DR
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16590 - Stat Rx Usa Llc
- 16590-648 - Divalproex Sodium
Product Characteristics
Product Packages
NDC Code 16590-648-30
Package Description: 30 TABLET, DELAYED RELEASE PARTICLES in 1 BOTTLE
NDC Code 16590-648-60
Package Description: 60 TABLET, DELAYED RELEASE PARTICLES in 1 BOTTLE
NDC Code 16590-648-90
Package Description: 90 TABLET, DELAYED RELEASE PARTICLES in 1 BOTTLE
Product Details
What is NDC 16590-648?
What are the uses for Divalproex Sodium DR?
Which are Divalproex Sodium DR 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 DR 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STARCH, CORN (UNII: O8232NY3SJ)
- POVIDONE K30 (UNII: U725QWY32X)
- HYPROMELLOSE (UNII: 3NXW29V3WO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- TALC (UNII: 7SEV7J4R1U)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
What is the NDC to RxNorm Crosswalk for Divalproex Sodium DR?
- RxCUI: 1099870 - divalproex sodium 500 MG Delayed 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".