NDC 53808-0266 Hydrochlorothiazide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53808 - State Of Florida Doh Central Pharmacy
- 53808-0266 - Hydrochlorothiazide
Product Characteristics
Product Packages
NDC Code 53808-0266-1
Package Description: 30 TABLET in 1 BLISTER PACK
Product Details
What is NDC 53808-0266?
What are the uses for Hydrochlorothiazide?
Which are Hydrochlorothiazide UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH)
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH) (Active Moiety)
Which are 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- CALCIUM STEARATE (UNII: 776XM7047L)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
What is the NDC to RxNorm Crosswalk for Hydrochlorothiazide?
- RxCUI: 310798 - hydroCHLOROthiazide 25 MG Oral Tablet
- RxCUI: 310798 - hydrochlorothiazide 25 MG Oral Tablet
- RxCUI: 310798 - HCTZ 25 MG 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".