NDC 16590-312 Diovan Hct
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16590 - Stat Rx Usa Llc
- 16590-312 - Diovan Hct
Product Characteristics
Product Packages
NDC Code 16590-312-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
NDC Code 16590-312-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
NDC Code 16590-312-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 16590-312?
What are the uses for Diovan Hct?
Which are Diovan Hct UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH)
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH) (Active Moiety)
- VALSARTAN (UNII: 80M03YXJ7I)
- VALSARTAN (UNII: 80M03YXJ7I) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Diovan Hct?
- RxCUI: 200284 - HCTZ 12.5 MG / valsartan 80 MG Oral Tablet
- RxCUI: 200284 - hydrochlorothiazide 12.5 MG / valsartan 80 MG Oral Tablet
- RxCUI: 809014 - Diovan HCT 80 MG / 12.5 MG Oral Tablet
- RxCUI: 809014 - hydrochlorothiazide 12.5 MG / valsartan 80 MG Oral Tablet [Diovan HCT]
- RxCUI: 809014 - Diovan HCT 80/12.5 (valsartan / HCTZ) 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".