NDC 16590-832 Gabitril
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16590 - Stat Rx Usa Llc
- 16590-832 - Gabitril
Product Characteristics
Product Packages
NDC Code 16590-832-30
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 16590-832-45
Package Description: 45 TABLET in 1 BOTTLE
NDC Code 16590-832-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 16590-832-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 16590-832?
What are the uses for Gabitril?
Which are Gabitril UNII Codes?
The UNII codes for the active ingredients in this product are:
- TIAGABINE HYDROCHLORIDE (UNII: DQH6T6D8OY)
- TIAGABINE (UNII: Z80I64HMNP) (Active Moiety)
Which are Gabitril 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:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSPOVIDONE (UNII: 68401960MK)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Gabitril?
- RxCUI: 1299903 - tiaGABine HCl 12 MG Oral Tablet
- RxCUI: 1299903 - tiagabine hydrochloride 12 MG Oral Tablet
- RxCUI: 1299967 - Gabitril 12 MG Oral Tablet
- RxCUI: 1299967 - tiagabine hydrochloride 12 MG Oral Tablet [Gabitril]
* 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".