NDC 54868-6452 Valsartan
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-6452 - Valsartan
Product Characteristics
ORANGE (C48331)
OVAL (C48345)
17 MM
7433;TEVA
Product Packages
NDC Code 54868-6452-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 54868-6452?
What are the uses for Valsartan?
Which are Valsartan UNII Codes?
The UNII codes for the active ingredients in this product are:
- VALSARTAN (UNII: 80M03YXJ7I)
- VALSARTAN (UNII: 80M03YXJ7I) (Active Moiety)
Which are Valsartan 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- CROSPOVIDONE (UNII: 68401960MK)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MANNITOL (UNII: 3OWL53L36A)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
What is the NDC to RxNorm Crosswalk for Valsartan?
- RxCUI: 349199 - valsartan 80 MG Oral Tablet
- RxCUI: 349200 - valsartan 320 MG Oral Tablet
- RxCUI: 349201 - valsartan 160 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".