NDC 76413-163 Folic Acid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
ORANGE (C48331)
Code Structure Chart
Product Details
What is NDC 76413-163?
What are the uses for Folic Acid?
Which are Folic Acid UNII Codes?
The UNII codes for the active ingredients in this product are:
- FOLIC ACID (UNII: 935E97BOY8)
- FOLIC ACID (UNII: 935E97BOY8) (Active Moiety)
Which are Folic 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:
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- STARCH, CORN (UNII: O8232NY3SJ)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- STEARIC ACID (UNII: 4ELV7Z65AP)
What is the NDC to RxNorm Crosswalk for Folic Acid?
- RxCUI: 310410 - folic acid 1 MG Oral Tablet
- RxCUI: 310410 - folate 1 MG Oral Tablet
- RxCUI: 310410 - vitamin B9 1,000 MCG 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".