NDC 69387-100 Amantadine Hcl
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What is NDC 69387-100?
What are the uses for Amantadine Hcl?
Which are Amantadine Hcl UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMANTADINE HYDROCHLORIDE (UNII: M6Q1EO9TD0)
- AMANTADINE (UNII: BF4C9Z1J53) (Active Moiety)
Which are Amantadine Hcl 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:
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- GELATIN (UNII: 2G86QN327L)
- GLYCERIN (UNII: PDC6A3C0OX)
- SOYBEAN OIL (UNII: 241ATL177A)
- SORBITOL (UNII: 506T60A25R)
- SORBITAN (UNII: 6O92ICV9RU)
- MANNITOL (UNII: 3OWL53L36A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WHITE WAX (UNII: 7G1J5DA97F)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
What is the NDC to RxNorm Crosswalk for Amantadine Hcl?
- RxCUI: 849389 - amantadine HCl 100 MG Oral Capsule
- RxCUI: 849389 - amantadine hydrochloride 100 MG Oral Capsule
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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".