NDC 53808-0804 Triamterene And Hydrochlorothiazide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53808 - State Of Florida Doh Central Pharmacy
- 53808-0804 - Triamterene And Hydrochlorothiazide
Product Characteristics
Product Packages
NDC Code 53808-0804-1
Package Description: 30 TABLET in 1 BLISTER PACK
Product Details
What is NDC 53808-0804?
What are the uses for Triamterene And Hydrochlorothiazide?
Which are Triamterene And Hydrochlorothiazide UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRIAMTERENE (UNII: WS821Z52LQ)
- TRIAMTERENE (UNII: WS821Z52LQ) (Active Moiety)
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH)
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH) (Active Moiety)
Which are Triamterene And Hydrochlorothiazide 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLACRILIN POTASSIUM (UNII: 0BZ5A00FQU)
- POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
- POVIDONE (UNII: FZ989GH94E)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Triamterene And Hydrochlorothiazide?
- RxCUI: 310818 - triamterene 75 MG / hydroCHLOROthiazide 50 MG Oral Tablet
- RxCUI: 310818 - hydrochlorothiazide 50 MG / triamterene 75 MG Oral Tablet
- RxCUI: 310818 - HCTZ 50 MG / triamterene 75 MG 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".