NDC 72189-010 Valproic Acid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72189 - Direct_rx
- 72189-010 - Valproic Acid
Product Characteristics
Product Packages
NDC Code 72189-010-30
Package Description: 30 CAPSULE in 1 BOTTLE
Product Details
What is NDC 72189-010?
What are the uses for Valproic Acid?
Which are Valproic Acid UNII Codes?
The UNII codes for the active ingredients in this product are:
- VALPROIC ACID (UNII: 614OI1Z5WI)
- VALPROIC ACID (UNII: 614OI1Z5WI) (Active Moiety)
Which are Valproic Acid 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:
- PEANUT OIL (UNII: 5TL50QU0W4)
- GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
- GLYCERIN (UNII: PDC6A3C0OX)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Valproic Acid?
- RxCUI: 1099681 - valproic acid 250 MG Oral Capsule
- RxCUI: 1099681 - VPA 250 MG Oral Capsule
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Patient Education
Valproic Acid
Valproic acid is used alone or with other medications to treat certain types of seizures. Valproic acid is also used to treat mania (episodes of frenzied, abnormally excited mood) in people with bipolar disorder (manic-depressive disorder; a disease that causes episodes of depression, episodes of mania, and other abnormal moods). It is also used to prevent migraine headaches but not to relieve headaches that have already begun. Valproic acid is in a class of medications called anticonvulsants. It works by increasing the amount of a certain natural substance in the brain.
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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".